Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_provenance.
- NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_assertion description "[The maternal MTHFR 677C > T variants are a risk factor for CHD in offspring, confined to conotruncal heart defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_provenance.
- NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_assertion evidence source_evidence_literature NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_provenance.
- NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_assertion SIO_000772 16524890 NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_provenance.
- NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_assertion wasDerivedFrom befree-2016 NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_provenance.
- NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_assertion wasGeneratedBy ECO_0000203 NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_provenance.