Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_assertion> ?p ?o ?g. }
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- NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_assertion type Assertion NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_head.
- NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_assertion description "[Our results do not support involvement of coding mutations in NR2E1 or SNX3 in MMEP or related phenotypes; however, we cannot exclude the possibility that regulatory NR2E1 or SNX3 mutations or deletions at this locus may underlie abnormal human cortical development in some patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_provenance.
- NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_assertion evidence source_evidence_literature NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_provenance.
- NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_assertion SIO_000772 17655765 NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_provenance.
- NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_assertion wasDerivedFrom befree-20140225 NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_provenance.
- NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_assertion wasGeneratedBy ECO_0000203 NP524588.RA2z6OLTuuA30kd3rXzkrnXqQmpbJcMenoLGLGO05NX7k130_provenance.