Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_assertion wasGeneratedBy ECO_0000203 NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_assertion wasDerivedFrom befree-20150227 NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_assertion SIO_000772 9627113 NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_assertion evidence source_evidence_literature NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_assertion description "[Investigation of mutations in exon 8, especially codon 273 mutation and mutant H2 alpha helix was considered to be a clinically useful approach for determining the prognosis of patients with NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.