Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_assertion> ?p ?o ?g. }
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- NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_assertion type Assertion NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_head.
- NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_assertion description "[Its most common occurrence is its association with ovarian cancer in the so-called hereditary breast-ovarian cancer syndrome due to BRCA1 and BRCA2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_provenance.
- NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_assertion evidence source_evidence_literature NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_provenance.
- NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_assertion SIO_000772 18086272 NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_provenance.
- NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_assertion wasDerivedFrom befree-2016 NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_provenance.
- NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_assertion wasGeneratedBy ECO_0000203 NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_provenance.