Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_provenance.
- NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_assertion description "[Huntington disease (HD) is a devastating neurologic disorder that is characterized by abnormal expansion of a CAG nt repeat in the first exon of the huntingtin (htt) gene, producing a mutant protein with an elongated polyglutamine stretch.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_provenance.
- NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_assertion evidence source_evidence_literature NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_provenance.
- NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_assertion SIO_000772 15737634 NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_provenance.
- NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_assertion wasDerivedFrom befree-2016 NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_provenance.
- NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_assertion wasGeneratedBy ECO_0000203 NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_provenance.
- befree-2016 importedOn "2016-02-19" NP483151.RAqHrH9ATIFHc8TA6tWXfaepirzx5zmMB1Vg2Y0Ec71fA130_provenance.