Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_assertion> ?p ?o ?g. }
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- NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_assertion type Assertion NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_head.
- NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_assertion wasGeneratedBy ECO_0000203 NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_provenance.
- NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_assertion wasDerivedFrom befree-2016 NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_provenance.
- NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_assertion SIO_000772 19500772 NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_provenance.
- NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_assertion evidence source_evidence_literature NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_provenance.
- NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_assertion description "[In contrast to the association of point mutations in FOXF1 with bowel malrotation, microdeletions of FOXF1 were associated with hypoplastic left heart syndrome and gastrointestinal atresias, probably due to haploinsufficiency for the neighboring FOXC2 and FOXL1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743460.RA0KkjVhnjhHTau90cKru1Eyvfd9FnUI_BVcMSvKUFNfM130_provenance.