Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_assertion> ?p ?o ?g. }
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- NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_assertion type Assertion NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_head.
- NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_assertion wasGeneratedBy ECO_0000203 NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_provenance.
- NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_assertion wasDerivedFrom befree-20140225 NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_provenance.
- NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_assertion SIO_000772 19500772 NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_provenance.
- NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_assertion evidence source_evidence_literature NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_provenance.
- NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_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." NP687436.RAPu-cSeJxrITnmC4DV65ZXHuGxt6lVSYUYdW4EPSTYS4130_provenance.