Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_provenance.
- NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_assertion wasGeneratedBy ECO_0000203 NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_provenance.
- NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_assertion wasDerivedFrom befree-20140225 NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_provenance.
- NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_assertion SIO_000772 18184292 NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_provenance.
- NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_assertion evidence source_evidence_literature NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_provenance.
- NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_assertion description "[The mutations responsible for hemiplegic migraine have been described in the CACNA1A gene (chromosome 19p13), ATP1A2 gene (chromosome 1q23), and SCN1A gene (chromosome 2q24).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP249518.RA6p70BUveBr2GsDX9rPb6qQkkNzL0mJNSuPIrSqDKpKo130_provenance.