Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_provenance.
- NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_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." NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_provenance.
- NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_assertion evidence source_evidence_literature NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_provenance.
- NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_assertion SIO_000772 15021241 NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_provenance.
- NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_assertion wasDerivedFrom befree-20140225 NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_provenance.
- NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_assertion wasGeneratedBy ECO_0000203 NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP815814.RAWhff_z1iiMrDFVOIP_RDDhKTayZ17vaNsNe4LwBwWvA130_provenance.