Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_provenance.
- befree-2016 importedOn "2016-02-19" NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_provenance.
- NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_assertion wasGeneratedBy ECO_0000203 NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_provenance.
- NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_assertion wasDerivedFrom befree-2016 NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_provenance.
- NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_assertion SIO_000772 11319193 NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_provenance.
- NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_assertion evidence source_evidence_literature NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_provenance.
- NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_assertion description "[Recent studies have shown that a common mutation (nucleotide 677 C-->T) in the methylenetetrahydrofolate reductase (MTHFR) gene may contribute to mild hyperhomocysteinemia and, therefore, to the incidence of coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315807.RAq0GCZjVeoQ-tVBJYcs3RIWC_Qso0tUVSrlhKDK3r8q0130_provenance.