Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_provenance.
- NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_assertion description "[Maternal, paternal, and fetal DNA were genotyped for the methylenetetrahydrofolate reductase (MTHFR) C677T and Factor V Leiden (FVL) G1691A SNPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_provenance.
- NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_assertion evidence source_evidence_literature NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_provenance.
- NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_assertion SIO_000772 15097012 NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_provenance.
- NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_assertion wasDerivedFrom befree-2016 NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_provenance.
- NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_assertion wasGeneratedBy ECO_0000203 NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_provenance.
- befree-2016 importedOn "2016-02-19" NP440761.RAh_NLQFucdEh3p1ym4KcGSnYwGedAxgWBrR79VsVjby4130_provenance.