Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_assertion type Assertion NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_head.
- NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_assertion description "[Haploinsufficiency of RAI1 results in Smith-Magenis syndrome (SMS), a disorder characterized by intellectual disability, multiple congenital anomalies, obesity, neurobehavioral abnormalities, and a disrupted circadian sleep-wake pattern.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_provenance.
- NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_assertion evidence source_evidence_literature NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_provenance.
- NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_assertion SIO_000772 22578325 NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_provenance.
- NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_assertion wasDerivedFrom befree-20150227 NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_provenance.
- NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_assertion wasGeneratedBy ECO_0000203 NP1002365.RATODhE7O1DjVFMP9m3DG4YcRHSUZWqihwsiO5k_fX9WU130_provenance.