Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_provenance.
- NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_assertion description "[To investigate if single nucleotide polymorphisms on chromosome 12p13 and within 11 kb of the gene NINJ2 would be associated with earlier-onset (vs. late-onset) first-ever ischemic stroke and increase silent cerebrovascular lesions prior to the manifestation of the stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_provenance.
- NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_assertion evidence source_evidence_literature NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_provenance.
- NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_assertion SIO_000772 22429733 NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_provenance.
- NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_assertion wasDerivedFrom befree-20140225 NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_provenance.
- NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_assertion wasGeneratedBy ECO_0000203 NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP292030.RAEXGHGO-WAOrbzYPdgj2AlhKjSeIdTSo1sStirbNbY-Y130_provenance.