Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_provenance.
- NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_assertion description "[PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_provenance.
- NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_assertion evidence source_evidence_literature NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_provenance.
- NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_assertion SIO_000772 22243967 NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_provenance.
- NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_assertion wasDerivedFrom befree-20150227 NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_provenance.
- NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_assertion wasGeneratedBy ECO_0000203 NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP963633.RAARL39h0FhgUxw3LM9wgahmjJwN8QiG2dga23yYxNiS8130_provenance.