Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_provenance.
- NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_assertion description "[Conversely, congenital heart defects, particularly mitral valve and septal defects, and ocular anomalies seem to be less frequent among MEK1/MEK2 mutation-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_provenance.
- NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_assertion evidence source_evidence_literature NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_provenance.
- NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_assertion SIO_000772 19156172 NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_provenance.
- NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_assertion wasDerivedFrom gad-20150221 NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_provenance.
- NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_assertion wasGeneratedBy ECO_0000203 NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP93736.RADtaGIW1aHdraGeNJ54VjMIARqDHRFtjnbEZ1YMQ7cGw130_provenance.