Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_provenance.
- NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_assertion description "[Twenty-five PTCs (11 with BRAF(V600E), 4 with RET/PTC1, and 10 without mutation in HRAS, KRAS, NRAS, BRAF, RET/PTC1, or RET/PTC3) were analyzed using Genome-Wide Human SNP Array 6.0 which allows us to detect copy number alteration (CNA) and uniparental disomy (UPD), also referred to as copy neutral loss of heterozygosity, in a single experiment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_provenance.
- NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_assertion evidence source_evidence_literature NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_provenance.
- NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_assertion SIO_000772 22558328 NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_provenance.
- NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_assertion wasDerivedFrom befree-20140225 NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_provenance.
- NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_assertion wasGeneratedBy ECO_0000203 NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP531832.RA-8Tw2IWp495oRLNwMK7jUCnik5NwZG7dfZM_B5To2yk130_provenance.