Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_provenance.
- NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_assertion description "[Patients with idiopathic PE tended to have a higher frequency of homozygous MTHFR sequence variants, but mean (SD) plasma homocysteine concentrations were not increased [15.6 (5.4) micromol/L vs 12.8 (4.6) micromol/L for homozygous, and wild-type, respectively; P = 0.40].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_provenance.
- NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_assertion evidence source_evidence_literature NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_provenance.
- NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_assertion SIO_000772 16574759 NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_provenance.
- NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_assertion wasDerivedFrom befree-20150227 NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_provenance.
- NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_assertion wasGeneratedBy ECO_0000203 NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP575187.RATt5RY3vQh28Rc0Q7D3sNVbp79Pok2SsEwnRFSghtQQE130_provenance.