Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion description "[Mutations in the CHRNA4 or CHRNB subunits of the neuronal nicotinic acetylcholine receptor lead to familial nocturnal frontal lobe epilepsy, while defects in the voltage-gated potassium channels KCNQ2 and KCNQ3 have recently been found to cause benign familial neonatal convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion evidence source_evidence_literature NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion SIO_000772 11888238 NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion wasDerivedFrom befree-20140225 NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_assertion wasGeneratedBy ECO_0000203 NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP881063.RAZxSsiACh6WgksPK5Q-qZeaCRwKeZD7ekvK4lV8_ma0s130_provenance.