Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_assertion> ?p ?o ?g. }
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- NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_assertion type Assertion NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_head.
- NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_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." NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_provenance.
- NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_assertion evidence source_evidence_literature NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_provenance.
- NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_assertion SIO_000772 10562279 NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_provenance.
- NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_assertion wasDerivedFrom befree-20140225 NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_provenance.
- NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_assertion wasGeneratedBy ECO_0000203 NP875702.RA7veGzjhmJBFM7s-vuvtZEhLnL564cXefN0zcSA3ANvQ130_provenance.