Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_provenance.
- NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_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." NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_provenance.
- NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_assertion evidence source_evidence_literature NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_provenance.
- NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_assertion SIO_000772 23047679 NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_provenance.
- NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_assertion wasDerivedFrom befree-20150227 NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_provenance.
- NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_assertion wasGeneratedBy ECO_0000203 NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP672451.RA9eRn7IUOt6DpndsPa1hyaO3JlcbqNS9dxh9glSo51CI130_provenance.