Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance.
- NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance.
- NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_assertion evidence source_evidence_literature NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance.
- NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_assertion SIO_000772 11739564 NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance.
- NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_assertion wasDerivedFrom befree-20140225 NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance.
- NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_assertion wasGeneratedBy ECO_0000203 NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP272815.RA6yNUmVGqUjupRSqyi4G5VFzYrvHy95O2ZcyGv1SpJl8130_provenance.