Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_provenance.
- NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_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." NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_provenance.
- NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_assertion evidence source_evidence_literature NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_provenance.
- NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_assertion SIO_000772 15737634 NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_provenance.
- NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_assertion wasDerivedFrom befree-20150227 NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_provenance.
- NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_assertion wasGeneratedBy ECO_0000203 NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP445352.RAK6LefeHlI4q4jEAUTgU5F8jwHy1CIHa9N4yOmJ4oXNg130_provenance.