Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_provenance.
- NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_assertion description "[Mutations in angiogenin (ANG), a member of the ribonuclease A superfamily, are associated with amyotrophic lateral sclerosis (ALS; sporadic and familial) and Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_provenance.
- NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_assertion evidence source_evidence_literature NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_provenance.
- NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_assertion SIO_000772 23047679 NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_provenance.
- NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_assertion wasDerivedFrom befree-20140225 NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_provenance.
- NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_assertion wasGeneratedBy ECO_0000203 NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP913981.RA1LfOBru0ZWohfxQ70RfXJO3ZNLCtuKBGwOsTipMWcgI130_provenance.