Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_provenance.
- NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_assertion description "[Contrary to previously described evidence the A1298C polymorphism in the MTHFR gene does not appear to modulate AO of HD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_provenance.
- NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_assertion evidence source_evidence_literature NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_provenance.
- NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_assertion SIO_000772 16372906 NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_provenance.
- NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_assertion wasDerivedFrom gad-20150221 NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_provenance.
- NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_assertion wasGeneratedBy ECO_0000203 NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP97988.RAQr8gWFc7kT1d2kWETwJKhQ0QV_53Q9rRaEnldf1AZrA130_provenance.