Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_provenance.
- NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_assertion description "[KRAS2 mutations were found in five out of 89 (6%) HNSCC examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_provenance.
- NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_assertion evidence source_evidence_literature NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_provenance.
- NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_assertion SIO_000772 12879021 NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_provenance.
- NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_assertion wasDerivedFrom befree-20150227 NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_provenance.
- NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_assertion wasGeneratedBy ECO_0000203 NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP528032.RAXIGZLRmYRvw2im0t5WyQLs1-IsqbcCCRtwknlpRFkrs130_provenance.