Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_provenance.
- NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_assertion description "[Analysis of common SNP-based haplotypes has revealed that most European HD subjects have distinguishable HTT haplotypes on their normal and disease chromosomes and that ?50% of the latter share the same major HD haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_provenance.
- NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_assertion evidence source_evidence_literature NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_provenance.
- NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_assertion SIO_000772 26320893 NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_provenance.
- NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_assertion wasDerivedFrom befree-2016 NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_provenance.
- NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_assertion wasGeneratedBy ECO_0000203 NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293453.RAwihSBtoMW23u2F7XTaEBUlhDpWgccQzh0E0wNELh0m0130_provenance.