Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_provenance.
- NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_assertion description "[Most importantly, we discovered that TRRAP harbored a recurrent mutation that clustered in one position (p. Ser722Phe) in 6 out of 167 affected individuals (?4%), as well as a previously unidentified gene, GRIN2A, which was mutated in 33% of melanoma samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_provenance.
- NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_assertion evidence source_evidence_literature NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_provenance.
- NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_assertion SIO_000772 21499247 NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_provenance.
- NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_assertion wasDerivedFrom befree-20150227 NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_provenance.
- NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_assertion wasGeneratedBy ECO_0000203 NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP794023.RAaGsyMlR58sOZj9qSTnNi0cO3vIT70V40RyeTi6evdeY130_provenance.