Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_assertion> ?p ?o ?g. }
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- NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_assertion type Assertion NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_head.
- NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_assertion wasGeneratedBy ECO_0000203 NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_provenance.
- NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_assertion wasDerivedFrom befree-20140225 NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_provenance.
- NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_assertion SIO_000772 19500772 NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_provenance.
- NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_assertion evidence source_evidence_literature NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_provenance.
- NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_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." NP330758.RATj0oymofrZul-1yL2pc7zQMXewsctdvETRPuWyLbYXI130_provenance.