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- source_evidence_literature type ECO_0000212 NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_provenance.
- NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_assertion description "[These patients were genotyped for vascular disease-associated polymorphisms in the genes coding for methylenetetrahydrofolate reductase (MTHFR), angiotensin-converting enzyme (ACE), factor V Leiden (FVL), and a common genetic risk factor for AD, apolipoprotein E epsilon4 (APOE epsilon4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_provenance.
- NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_assertion evidence source_evidence_literature NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_provenance.
- NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_assertion SIO_000772 9660395 NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_provenance.
- NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_assertion wasDerivedFrom befree-20150227 NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_provenance.
- NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_assertion wasGeneratedBy ECO_0000203 NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP350092.RAbQNsLvH2odIsjFc1GEhHHVDJJGI_KMNMJnJbe6t--EU130_provenance.