Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance.
- NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance.
- NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_assertion evidence source_evidence_literature NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance.
- NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_assertion SIO_000772 24569455 NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance.
- NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_assertion wasDerivedFrom befree-20150227 NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance.
- NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_assertion wasGeneratedBy ECO_0000203 NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP650564.RAo1AmZZd4NNgH2fXGq86VlEbVtgvOgYHqept3C9A3Ieg130_provenance.