Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_assertion> ?p ?o ?g. }
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- NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_assertion type Assertion NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_head.
- NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_assertion description "[Up to 75% of FHM families have a mutation in the P/Q-type calcium channel Ca(v)2.1 subunit CACNA1A gene on chromosome 19p13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_provenance.
- NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_assertion evidence source_evidence_literature NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_provenance.
- NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_assertion SIO_000772 12953268 NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_provenance.
- NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_assertion wasDerivedFrom befree-2016 NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_provenance.
- NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_assertion wasGeneratedBy ECO_0000203 NP407610.RAvGB_y_L_pXWeDPgEf27oKaW95Ui2R5hJeOX1yPB1CHs130_provenance.