Title: BioCypher graph schema configuration file # --- # "Named Things" # --- protein: represented_as: node preferred_id: uniprot input_label: protein db_collection_name: proteins properties: name: str score: float taxon: int genes: str[] microRNA: represented_as: node preferred_id: mirbase.mature input_label: mirna complex: synonym_for: macromolecular complex represented_as: node preferred_id: complexportal input_label: complex pathway: represented_as: node preferred_id: [reactome, wikipathways] input_label: [reactome, wikipathways] gene: represented_as: node preferred_id: hgnc input_label: [hgnc, ensg] exclude_properties: accession disease: represented_as: node preferred_id: doid input_label: Disease side effect: is_a: phenotypic feature represented_as: node preferred_id: sider.effect input_label: sider sequence variant: represented_as: node preferred_id: [clinically relevant, known, somatic] input_label: [Clinically_relevant_variant, Known_variant, Somatic_mutation] properties: source: str original_source: str effect: str biotype: str snRNA sequence: is_a: nucleic acid entity represented_as: node preferred_id: [intact, rnacentral] input_label: [intact_snrna, rnacentral_snrna] properties: ac: str fullName: str shortName: str preferredName: str exclude_properties: sequence DNA sequence: is_a: nucleic acid entity represented_as: node preferred_id: ensembl input_label: dna properties: ac: str fullName: str shortName: str preferredName: str sequence: str dsDNA sequence: is_a: [DNA sequence, nucleic acid entity] inherit_properties: True represented_as: node preferred_id: [intact, uniparc] input_label: [intact_dsdna, uniprot_archive_dsdna] # --- # Associations # --- post translational interaction: is_a: pairwise molecular interaction represented_as: node label_as_edge: INTERACTS_POST_TRANSLATIONAL input_label: post_translational phosphorylation: is_a: post translational interaction represented_as: edge input_label: phosphorylation gene to disease association: represented_as: edge label_as_edge: PERTURBED_IN_DISEASE input_label: [protein_disease, gene_disease] exclude_properties: accession mutation to tissue association: is_a: [genotype to tissue association, entity to tissue association, association] represented_as: edge label_as_edge: Is_Mutated_In input_label: Gene_Is_Mutated_In_Cell_Tissue variant to gene association: # -> Known.... and Somatic.... represented_as: edge source: [known.sequence variant, somatic.sequence variant] target: gene input_label: [ VARIANT_FOUND_IN_GENE_Known_variant_Gene, VARIANT_FOUND_IN_GENE_Somatic_mutation_Gene ] gene to gene association: represented_as: edge input_label: gene_gene properties: directional: bool curated: bool score: float id: str # should be removed gene to variant association: # should be removed is_a: gene to variant association represented_as: edge input_label: gene_variant