Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_assertion type Assertion NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_head.
- NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_assertion wasGeneratedBy ECO_0000203 NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance.
- NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_assertion wasDerivedFrom befree-20150227 NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance.
- NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_assertion SIO_000772 22512561 NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance.
- NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_assertion evidence source_evidence_literature NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance.
- NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_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." NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance.