Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_assertion type Assertion NP539220.RAPg6s4vq8oKF4XM202J9uBBQfp8oRAaWVBHDNAuf-2-Y130_head.
- 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.