Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_provenance.
- NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_assertion description "[The 3'-UTR contains a polymorphic AGG repeat that appears not to be expanded in patients suffering from different neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_provenance.
- NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_assertion evidence source_evidence_literature NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_provenance.
- NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_assertion SIO_000772 9811930 NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_provenance.
- NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_assertion wasDerivedFrom befree-20140225 NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_provenance.
- NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_assertion wasGeneratedBy ECO_0000203 NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_provenance.
- befree-20140225 importedOn "2014-02-25" NP870886.RA3WSuu0KMF-gEFhoXZaR7d-7HYvK0XmkV_jrNO6imE80130_provenance.