Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_provenance.
- NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_assertion description "[A mutation in the ATP1A2 sodium potassium ATPase pump gene has been described in a family in which familial hemiplegic migraine and benign familial infantile convulsions partly co-segregate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_provenance.
- NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_assertion evidence source_evidence_literature NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_provenance.
- NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_assertion SIO_000772 15021241 NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_provenance.
- NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_assertion wasDerivedFrom befree-20150227 NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_provenance.
- NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_assertion wasGeneratedBy ECO_0000203 NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256063.RAC4E0VBOGXc_vAcBw0AGQhzuGRztIT9l7n6V5FYwwk8E130_provenance.