Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_provenance.
- NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_assertion description "[Gene mutations associated with epilepsy are known, to date, only for two disorders: the lissencephaly 1 gene in Miller-Dieker syndrome and mutations in the UBE3A gene in Angelman syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_provenance.
- NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_assertion evidence source_evidence_literature NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_provenance.
- NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_assertion SIO_000772 11579431 NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_provenance.
- NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_assertion wasDerivedFrom befree-20150227 NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_provenance.
- NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_assertion wasGeneratedBy ECO_0000203 NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_provenance.
- befree-20150227 importedOn "2015-02-27" NP605903.RA6Q6x1jjktfohip_IG7kTMTaTofsqmPDWjPWCPiWyHec130_provenance.