Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_assertion> ?p ?o ?g. }
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- NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_assertion type Assertion NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_head.
- NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_assertion description "[We suggest that the absence of the ZDHHC15 transcripts in this patient contributes to her phenotype, and that the gene is a strong candidate for nonsyndromic XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_provenance.
- NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_assertion evidence source_evidence_literature NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_provenance.
- NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_assertion SIO_000772 15915161 NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_provenance.
- NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_assertion wasDerivedFrom befree-20140225 NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_provenance.
- NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_assertion wasGeneratedBy ECO_0000203 NP212905.RAZX7MEjiCeer9LBlKHlx76WtsEcC6a9pOuP3dC8IScwo130_provenance.