Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_provenance.
- NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_assertion description "[Mutations responsible for autosomal dominant nocturnal frontal lobe epilepsy have been identified in two members of the neuronal nicotinic acetylcholine receptor gene family: CHRNA4(ENFL1 locus) and CHRNB2 (ENFL3 locus) coding for alpha4 and beta2 subunit, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_provenance.
- NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_assertion evidence source_evidence_literature NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_provenance.
- NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_assertion SIO_000772 15245761 NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_provenance.
- NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_assertion wasDerivedFrom befree-20140225 NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_provenance.
- NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_assertion wasGeneratedBy ECO_0000203 NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP557655.RAw_FiXq4KDCpo2ayohZXYHDtYHIENgyp1gs-XDpt69uQ130_provenance.