Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_assertion> ?p ?o ?g. }
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- NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_assertion type Assertion NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_head.
- NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_assertion description "[Mutations in human PEX12 result in Zellweger syndrome, a lethal neurological disorder, and implicate the zinc ring domain in PEX12 function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_provenance.
- NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_assertion evidence source_evidence_literature NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_provenance.
- NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_assertion SIO_000772 10562279 NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_provenance.
- NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_assertion wasDerivedFrom befree-2016 NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_provenance.
- NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_assertion wasGeneratedBy ECO_0000203 NP267657.RAX-lZ8wi1fMsi-iX1VMaXdECVUel4de8G12LOiMeh520130_provenance.