Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_provenance.
- NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_assertion description "[Six different mutations (12%) were detected in exon 2 of p16 (common to p16alpha and p16beta), in five out of 21 squamous lesions (24%) (one AK and four SCCs) and one out of 28 BCCs (3.5%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_provenance.
- NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_assertion evidence source_evidence_literature NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_provenance.
- NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_assertion SIO_000772 10498902 NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_provenance.
- NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_assertion wasDerivedFrom befree-2016 NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_provenance.
- NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_assertion wasGeneratedBy ECO_0000203 NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_provenance.
- befree-2016 importedOn "2016-02-19" NP264004.RAVNu3E_QIGgSViACvUmlYBNFJgU4wjbImy2DxBbHTwcw130_provenance.