Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_provenance.
- NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_assertion description "[Several other genetic regions including variants of CHEK2 (22q12), TP53BP1 (15q15) and RAD52 (12p13) have been demonstrated to influence lung cancer risk in candidate- or pathway-based analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_provenance.
- NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_assertion evidence source_evidence_literature NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_provenance.
- NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_assertion SIO_000772 22899653 NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_provenance.
- NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_assertion wasDerivedFrom befree-20140225 NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_provenance.
- NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_assertion wasGeneratedBy ECO_0000203 NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP915703.RAUcs4UXSYHlOsz4g-mCAZHZMows8_BeqOUZOTmVuFr2k130_provenance.