Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance.
- NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_assertion wasGeneratedBy ECO_0000203 NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance.
- NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_assertion wasDerivedFrom befree-2016 NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance.
- NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_assertion SIO_000772 24935154 NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance.
- NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_assertion evidence source_evidence_literature NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance.
- NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_assertion description "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance.