Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_provenance.
- NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_assertion description "[Huntington disease (HD) is a neurodegenerative disorder resulting from the expansion of a CAG trinucleotide repeat in the huntingtin (HTT) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_provenance.
- NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_assertion evidence source_evidence_literature NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_provenance.
- NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_assertion SIO_000772 23463025 NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_provenance.
- NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_assertion wasDerivedFrom befree-2016 NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_provenance.
- NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_assertion wasGeneratedBy ECO_0000203 NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1058046.RA715A01ppIQfaouUPb48TS8LvJYpbXachjyhfrLtJ3ZY130_provenance.