Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_assertion type Assertion NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_head.
- NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_assertion description "[Familial hemiplegic migraine (FHM) is genetically heterogeneous with mutations in the CACNA1A (FHM1), ATP1A2 (FHM2) and SCN1A (FHM3) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_provenance.
- NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_assertion evidence source_evidence_literature NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_provenance.
- NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_assertion SIO_000772 18451712 NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_provenance.
- NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_assertion wasDerivedFrom befree-20140225 NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_provenance.
- NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_assertion wasGeneratedBy ECO_0000203 NP557887.RAs3e7s7FwJSsxDDcaHU9w1MEHLzcHwLfgN-lcVzszTBU130_provenance.