Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_provenance.
- NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_assertion description "[Determination of MTHFR polymorphisms and CAG repeats enables screening for subjects with putative early HD onset in order to study neuroprotective compounds in their efficacy to delay HD symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_provenance.
- NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_assertion evidence source_evidence_literature NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_provenance.
- NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_assertion SIO_000772 15354395 NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_provenance.
- NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_assertion wasDerivedFrom gad-20150221 NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_provenance.
- NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_assertion wasGeneratedBy ECO_0000203 NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP130878.RA5urTfbX6sFePjacNYVJtFkR9dCtf0e6v0HUQ-s4VVvo130_provenance.