Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_provenance.
- NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_assertion description "[study showed that FGFR3 mutations appear to be common genetic alterations in multiple seborrheic keratoses with a varying interindividual mutation frequency but without specific intraindividual hot spots ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_provenance.
- NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_assertion evidence source_evidence_literature NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_provenance.
- NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_assertion SIO_000772 17392824 NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_provenance.
- NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_assertion wasDerivedFrom lhgdn-20090331 NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_provenance.
- NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_assertion wasGeneratedBy ECO_0000203 NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP151079.RApNwNClbahoRgZmhCH69b2U_lWSX3kReKDYYG8hru0Zs130_provenance.