Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_provenance.
- befree-2016 importedOn "2016-02-19" NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_provenance.
- NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_assertion wasGeneratedBy ECO_0000203 NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_provenance.
- NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_assertion wasDerivedFrom befree-2016 NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_provenance.
- NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_assertion SIO_000772 21204806 NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_provenance.
- NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_assertion evidence source_evidence_literature NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_provenance.
- NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_assertion description "[The band 2q24 constitutes the smallest commonly deleted segment in these patients, and contains the voltage-gated sodium channel genes SCN1A and SCN2A, associated with Dravet syndrome and benign familial neonatal-infantile seizures, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862969.RAKcn_yBXRM1av0PIrHW3Ny5VifCMa7AS8jSTeptfhSTU130_provenance.