Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_provenance.
- NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_assertion description "[To compare genetic test results for deleterious mutations of BRCA1 and BRCA2 with estimated probabilities of carrying such mutations; to assess sensitivity of genetic testing; and to assess the relevance of other susceptibility genes in familial breast and ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_provenance.
- NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_assertion evidence source_evidence_literature NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_provenance.
- NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_assertion SIO_000772 12039933 NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_provenance.
- NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_assertion wasDerivedFrom befree-2016 NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_provenance.
- NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_assertion wasGeneratedBy ECO_0000203 NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_provenance.
- befree-2016 importedOn "2016-02-19" NP356533.RAnxi4Nb4xJg12UCcQQyeL7X9Xs5K9KXrmVYCmnwDqJ-g130_provenance.