Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_assertion> ?p ?o ?g. }
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- NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_assertion type Assertion NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_head.
- NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_provenance.
- NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_assertion evidence source_evidence_literature NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_provenance.
- NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_assertion SIO_000772 11439091 NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_provenance.
- NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_assertion wasDerivedFrom befree-20140225 NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_provenance.
- NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_assertion wasGeneratedBy ECO_0000203 NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_provenance.