Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_provenance.
- NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_assertion wasGeneratedBy ECO_0000203 NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_provenance.
- NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_assertion wasDerivedFrom befree-20150227 NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_provenance.
- NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_assertion SIO_000772 19139296 NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_provenance.
- NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_assertion evidence source_evidence_literature NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_provenance.
- NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_assertion description "[Mutations in the central nervous system-specific voltage-gated sodium channel alpha1 subunit gene (SCN1A) lead not only to seizure syndromes but also to familial hemiplegic migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682485.RAXk-dJ_Nv_-yeqzKGn7qb5coP6T1kPht_1Ts7y9nSDFI130_provenance.