Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_provenance.
- NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_assertion description "[Furthermore, more frequent, but less penetrant, mutations have been identified in families with breast cancer clustering, in moderate or low penetrant genes, such as CHEK2, ATM, PALB2, and BRIP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_provenance.
- NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_assertion evidence source_evidence_literature NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_provenance.
- NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_assertion SIO_000772 23586058 NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_provenance.
- NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_assertion wasDerivedFrom befree-20150227 NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_provenance.
- NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_assertion wasGeneratedBy ECO_0000203 NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_provenance.
- befree-20150227 importedOn "2015-02-27" NP940439.RAEGZhHLWSBfXYvHRoyp0GUIgTlVZbSsEgTbiStpR22ls130_provenance.