Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_provenance.
- NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_assertion description "[BRAF mutations (V600E) were observed in 45.8% (11 of 24) of HPs, 60.9% (14 of 23) of SSAs, and 63.6% (7 of 11) of SSANs, and were equally found in both SSA and carcinoma/HGD areas of the individual SSANs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_provenance.
- NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_assertion evidence source_evidence_literature NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_provenance.
- NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_assertion SIO_000772 21263251 NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_provenance.
- NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_assertion wasDerivedFrom befree-20140225 NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_provenance.
- NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_assertion wasGeneratedBy ECO_0000203 NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP454508.RAtKDT80HivqeyJNnX4w6FASV80Qf2f04tAUFDkhdlVXc130_provenance.