Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_provenance.
- NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_assertion description "[The subjects included 734 patients with SCA (480 patients with sporadic SCA and 254 patients with familial SCA) without CAG repeat expansions at the SCA1, SCA2, Machado-Joseph disease, SCA6, SCA7, or dentatorubral-pallidolluysian atrophy loci, with 162 healthy subjects, 216 patients with Parkinson disease, and 195 with Alzheimer disease as control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_provenance.
- NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_assertion evidence source_evidence_literature NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_provenance.
- NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_assertion SIO_000772 14967767 NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_provenance.
- NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_assertion wasDerivedFrom befree-20150227 NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_provenance.
- NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_assertion wasGeneratedBy ECO_0000203 NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681695.RA_vlJQclrWvrGEavJHgKEF4RkiSttZoXdUXFWu3oTTYY130_provenance.