Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_assertion> ?p ?o ?g. }
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- NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_assertion type Assertion NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_head.
- NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_assertion description "[These results allow further delineation of the spectrum of malformations ascribed to SMADIP1 haploinsufficiency, which includes frequent features such as hypospadias and agenesis of the corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_provenance.
- NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_assertion evidence source_evidence_literature NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_provenance.
- NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_assertion SIO_000772 11595972 NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_provenance.
- NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_assertion wasDerivedFrom befree-20140225 NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_provenance.
- NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_assertion wasGeneratedBy ECO_0000203 NP165074.RAoh0BT8zDnDKaV7DvMDx1Ab-TX95mxng7J-kwExPURSQ130_provenance.