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- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion type Assertion NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_head.
- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion description "[Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion evidence source_evidence_curated NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion SIO_000772 9539740 NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion wasDerivedFrom ctd_human-20150221 NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion wasGeneratedBy ECO_0000218 NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.