Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_assertion> ?p ?o ?g. }
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- NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_assertion type Assertion NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_head.
- NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_assertion description "[A novel RAB27A mutation in a patient with Griscelli syndrome type 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_provenance.
- NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_assertion evidence source_evidence_literature NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_provenance.
- NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_assertion SIO_000772 21314004 NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_provenance.
- NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_assertion wasDerivedFrom befree-2016 NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_provenance.
- NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_assertion wasGeneratedBy ECO_0000203 NP871756.RAAlTGnd0i76UcunRdkYiAw1YV3x4S1pwvM3ZBddBcj_A130_provenance.