Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_assertion type Assertion NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_head.
- NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_assertion wasGeneratedBy ECO_0000203 NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_provenance.
- NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_assertion wasDerivedFrom befree-2016 NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_provenance.
- NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_assertion SIO_000772 20080591 NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_provenance.
- NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_assertion evidence source_evidence_literature NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_provenance.
- NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_assertion description "[Familial hemiplegic migraine (FHM)-causing mutations in the gene encoding the P/Q Ca(2+) channel alpha(1A) subunit (CACNA1A) locate to the pore and voltage sensor regions and normally involve gain-of-channel function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_provenance.