Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_provenance.
- NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_assertion wasGeneratedBy ECO_0000203 NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_provenance.
- NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_assertion wasDerivedFrom befree-20150227 NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_provenance.
- NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_assertion SIO_000772 24991435 NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_provenance.
- NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_assertion evidence source_evidence_literature NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_provenance.
- NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_assertion description "[Carriers of the TT and the CC genotype of the MTHFR C677T polymorphism seem to have an increased risk of the HELLP syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575518.RA1E0K6JLL-fPLvcv-BvsINgdKQjD2ZORuXeApZunuy9Q130_provenance.