Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_provenance.
- NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_assertion description "[Here we describe identification of the causative gene in autosomal-dominant partial epilepsy with auditory features (ADPEAF, MIM 600512), a rare form of idiopathic lateral temporal lobe epilepsy characterized by partial seizures with auditory disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_provenance.
- NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_assertion evidence source_evidence_literature NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_provenance.
- NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_assertion SIO_000772 11810107 NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_provenance.
- NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_assertion wasDerivedFrom befree-20140225 NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_provenance.
- NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_assertion wasGeneratedBy ECO_0000203 NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP813394.RAN-QFzhPgy4DPWpGPbYzB5u2RpWzDL5MtRAkbDObtb_M130_provenance.