Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP645689.RAc4UHXIJ9rAbLXeL2nvCAsLUiSPKuDtQpZWN6G6SREjY130_provenance.