Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_assertion type Assertion NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_head.
- NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_assertion wasGeneratedBy ECO_0000203 NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_provenance.
- NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_assertion wasDerivedFrom lhgdn-20090331 NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_provenance.
- NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_assertion SIO_000772 18184292 NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_provenance.
- NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_assertion evidence source_evidence_literature NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_provenance.
- NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_assertion description "[D999H is a novel Hemiplegic Migraine, Familial ATP1A2 mutation in an Irish family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205340.RAnOBiju3UpCWls3xCvKWyUpEAeXLN8DHRUZyiqpvx-JE130_provenance.