Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_assertion> ?p ?o ?g. }
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- NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_assertion type Assertion NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_head.
- NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_assertion description "[Our data exclude the responsibility of the pM5, MRP1 and NPIP genes in PXE, and strongly suggest that mutations in the last remaining candidate gene, MRP6, which encodes a 1503 amino-acid ABC membrane transporter, are the genetic defect responsible for PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_provenance.
- NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_assertion evidence source_evidence_literature NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_provenance.
- NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_assertion SIO_000772 11139250 NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_provenance.
- NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_assertion wasDerivedFrom befree-20140225 NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_provenance.
- NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_assertion wasGeneratedBy ECO_0000203 NP799831.RAwQdkHtZhHe5ao4h2rqCEKCEjPw1_n7dSkX3caopiQ8E130_provenance.