Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_provenance.
- NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_assertion description "[In conclusion, homozygosity for the C677T mutation in the MTHFR gene does not constitute a genetic risk factor for coronary artery diseases and neural tube defects in the Indonesian Javanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_provenance.
- NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_assertion evidence source_evidence_literature NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_provenance.
- NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_assertion SIO_000772 12594357 NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_provenance.
- NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_assertion wasDerivedFrom befree-2016 NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_provenance.
- NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_assertion wasGeneratedBy ECO_0000203 NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_provenance.
- befree-2016 importedOn "2016-02-19" NP384369.RA3G-FVkfGIhKdRIC6S5GSKX3FMy_0sqhU1JDyIT-wcPI130_provenance.