Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance.
- NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_assertion description "[To identify the genetic modifier(s) that might alter the age at onset in Huntington's disease (HD) we have analyzed variations in GluR6 kainate receptor (GluR6), CA150 gene, Delta2642 and polymorphic CCG repeat variation in huntingtin (htt) gene in 77 HD patients and normal individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance.
- NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_assertion evidence source_evidence_literature NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance.
- NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_assertion SIO_000772 12821179 NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance.
- NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_assertion wasDerivedFrom befree-20140225 NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance.
- NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_assertion wasGeneratedBy ECO_0000203 NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance.