Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_provenance.
- NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_assertion description "[Rare high-penetrance factors are expressed in familial clustering of melanoma and include mutations in CDKN2A (encoding p16(INK4a) and p14(ARF)) and CDK4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_provenance.
- NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_assertion evidence source_evidence_literature NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_provenance.
- NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_assertion SIO_000772 19585149 NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_provenance.
- NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_assertion wasDerivedFrom befree-20140225 NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_provenance.
- NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_assertion wasGeneratedBy ECO_0000203 NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_provenance.
- befree-20140225 importedOn "2014-02-25" NP774266.RAbFHEb12E5ik6seUD1einPP6Wc5aLn4-NEPLx2XLkqno130_provenance.