Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_provenance.
- NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_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." NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_provenance.
- NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_assertion evidence source_evidence_literature NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_provenance.
- NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_assertion SIO_000772 15021241 NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_provenance.
- NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_assertion wasDerivedFrom befree-20150227 NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_provenance.
- NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_assertion wasGeneratedBy ECO_0000203 NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP356499.RAJ3bpYODTJDzGqBTOuFA0QXNGQ1PjOtiaRiBgtcPU1iQ130_provenance.