Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance.
- 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.