Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_assertion> ?p ?o ?g. }
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- NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_assertion type Assertion NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_head.
- NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_assertion wasGeneratedBy ECO_0000203 NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_provenance.
- NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_assertion wasDerivedFrom befree-2016 NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_provenance.
- NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_assertion SIO_000772 22512561 NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_provenance.
- NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_assertion evidence source_evidence_literature NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_provenance.
- NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_provenance.