Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_provenance.
- NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_assertion description "[AL-DNA adducts were present in the renal cortex of 83% of patients with A:T to T:A mutations in TP53, FGFR3, or HRAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_provenance.
- NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_assertion evidence source_evidence_literature NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_provenance.
- NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_assertion SIO_000772 22493262 NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_provenance.
- NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_assertion wasDerivedFrom befree-20140225 NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_provenance.
- NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_assertion wasGeneratedBy ECO_0000203 NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP803471.RAKTHS-DomsDWtlFkyvAuEOZbV7av-VD1dKDPqYJHTdgc130_provenance.