Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_provenance.
- NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_assertion description "[Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_provenance.
- NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_assertion evidence source_evidence_curated NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_provenance.
- NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_assertion SIO_000772 10762541 NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_provenance.
- NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_assertion wasDerivedFrom uniprot-20150221 NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_provenance.
- NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_assertion wasGeneratedBy ECO_0000218 NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP38.RAPYxK4wHLj56YkE9cNDIB0z-P6Xhm2d_rfFr4SePgOH8130_provenance.