Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_assertion> ?p ?o ?g. }
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- NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_assertion type Assertion NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_head.
- NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_assertion description "[The PEX1 gene, which encodes a cytoplasmic AAA ATPase, is the responsible gene in more than half of the Zellweger syndrome spectrum patients, and mutations in PEX1 can account for the full spectrum of phenotypes seen in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_provenance.
- NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_assertion evidence source_evidence_literature NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_provenance.
- NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_assertion SIO_000772 10480353 NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_provenance.
- NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_assertion wasDerivedFrom befree-20140225 NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_provenance.
- NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_assertion wasGeneratedBy ECO_0000203 NP411996.RAK2GYVrXSIx7u70c7eUSjvCKkee276AzLDnIJ-bOrRdk130_provenance.