Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_provenance.
- NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_assertion wasGeneratedBy ECO_0000203 NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_provenance.
- NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_assertion wasDerivedFrom befree-20140225 NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_provenance.
- NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_assertion SIO_000772 20660572 NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_provenance.
- NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_assertion evidence source_evidence_literature NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_provenance.
- NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_assertion description "[All patients provided blood DNA for testing of the MEN1 and VHL genes for intragenic mutations and large deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP449555.RAU6w0MtJj82mxbAL49rHv30W3acvSzotpRwrFtMvfX2A130_provenance.