Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_assertion> ?p ?o ?g. }
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- NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_assertion type Assertion NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_head.
- NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_assertion description "[As the proteolipid protein gene (PLP) is within this region and mutations have been shown to be associated with non-classical PMD (Pelizaeus-Merzbacher disease), such as complex X linked hereditary spastic paraplegia, PLP may represent a candidate gene for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_provenance.
- NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_assertion evidence source_evidence_literature NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_provenance.
- NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_assertion SIO_000772 7643352 NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_provenance.
- NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_assertion wasDerivedFrom befree-2016 NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_provenance.
- NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_assertion wasGeneratedBy ECO_0000203 NP1316315.RAQ7Q2eQUIO5XHzvKaSH5-nNod79hG1AIso44C09gjj1M130_provenance.