Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_provenance.
- NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_assertion description "[Mutation of LGI1 gene has been identified in familial lateral temporal lobe epilepsy while mutations of genes which encode sodium channels and GABAA receptors have been reported in generalized epilepsy with febrile seizure plus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_provenance.
- NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_assertion evidence source_evidence_literature NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_provenance.
- NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_assertion SIO_000772 17981785 NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_provenance.
- NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_assertion wasDerivedFrom befree-2016 NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_provenance.
- NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_assertion wasGeneratedBy ECO_0000203 NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_provenance.
- befree-2016 importedOn "2016-02-19" NP638711.RAEExj2CJTp6YvB2E3Ovaj1DNKq-bQbw81wfI4fBY_VFE130_provenance.