Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_provenance.
- NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_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." NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_provenance.
- NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_assertion evidence source_evidence_literature NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_provenance.
- NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_assertion SIO_000772 15354395 NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_provenance.
- NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_assertion wasDerivedFrom befree-2016 NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_provenance.
- NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_assertion wasGeneratedBy ECO_0000203 NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_provenance.
- befree-2016 importedOn "2016-02-19" NP458971.RA23STLQRYoI9E3taHPMZN15Gq_t20kdT1FQ0iVf8n0ao130_provenance.