Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_assertion> ?p ?o ?g. }
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- NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_assertion type Assertion NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_head.
- NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_assertion wasGeneratedBy ECO_0000203 NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_provenance.
- NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_assertion wasDerivedFrom befree-20150227 NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_provenance.
- NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_assertion SIO_000772 11257260 NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_provenance.
- NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_assertion evidence source_evidence_literature NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_provenance.
- NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_provenance.