Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_provenance.
- NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_assertion description "[Homozygosity for the C677T mutation in the MTHFR gene does not constitute a genetic risk factor for coronary diseases and neural tube defects in the Indonesian Javanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_provenance.
- NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_assertion evidence source_evidence_literature NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_provenance.
- NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_assertion SIO_000772 12594357 NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_provenance.
- NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_assertion wasDerivedFrom lhgdn-20090331 NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_provenance.
- NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_assertion wasGeneratedBy ECO_0000203 NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198283.RAthTXwgcVjmLbvfL7IrJfxawhStxfM6lG0SeL8dh1bUs130_provenance.