Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_provenance.
- NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_assertion description "[A common mutation in methylenetetrahydrofolate reductase (MTHFR), 677C-->T, is associated with reduced enzyme activity, a thermolabile enzyme and mild hyperhomocysteinemia, a risk factor for vascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_provenance.
- NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_assertion evidence source_evidence_literature NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_provenance.
- NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_assertion SIO_000772 11395038 NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_provenance.
- NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_assertion wasDerivedFrom befree-2016 NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_provenance.
- NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_assertion wasGeneratedBy ECO_0000203 NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_provenance.
- befree-2016 importedOn "2016-02-19" NP320164.RAP52A4_nEP4DIXY9T0gPceN-3Kni59eXDDQsDgvt_xvA130_provenance.