Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_provenance.
- NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_assertion description "[Determination of MTHFR polymorphisms and CAG repeat lengths enables screening for subjects with putative early Huntington's disease onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_provenance.
- NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_assertion evidence source_evidence_literature NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_provenance.
- NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_assertion SIO_000772 15354395 NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_provenance.
- NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_assertion wasDerivedFrom lhgdn-20090331 NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_provenance.
- NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_assertion wasGeneratedBy ECO_0000203 NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP206711.RAiZ3tPkGSS_MHMmTxyWrr0LgcSyD1zkiQLl1LE65gWaQ130_provenance.