Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_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." NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance.
- NP25752.RA1j-bySlq-RKVPk_0ndwKI2SuG0FKLVUr8HcFzeCpNFU130_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." NP25752.RA1j-bySlq-RKVPk_0ndwKI2SuG0FKLVUr8HcFzeCpNFU130_provenance.
- NP4879.RANxOQK-Doq6e44gtrVay7Cke_HT-6McXSouQtE3fWGek130_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." NP4879.RANxOQK-Doq6e44gtrVay7Cke_HT-6McXSouQtE3fWGek130_provenance.
- NP25749.RAOh7SS8i3VLE-ALNwnVA4qtUtnRe-9C8FxKKnPlD5CH4130_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." NP25749.RAOh7SS8i3VLE-ALNwnVA4qtUtnRe-9C8FxKKnPlD5CH4130_provenance.
- 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.
- 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." provenance.
- 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." provenance.
- 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." provenance.
- 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." provenance.
- 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." provenance.
- NP1392747.RAULunsrmJSyO5-DM1ruRJGRvd1VOR0DtoBRqm0fd4Kdc130_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." NP1392747.RAULunsrmJSyO5-DM1ruRJGRvd1VOR0DtoBRqm0fd4Kdc130_provenance.
- NP9702.RAkZnuxvHG4nn_ME302-GvvIArsEZY3YQJMMmm_ua1iTM130_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." NP9702.RAkZnuxvHG4nn_ME302-GvvIArsEZY3YQJMMmm_ua1iTM130_provenance.
- NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_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." NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance.
- NP37791.RAK-MWIpctBYurf83sru3mp9syWVDdFvIj0n65YUWBqjY130_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." NP37791.RAK-MWIpctBYurf83sru3mp9syWVDdFvIj0n65YUWBqjY130_provenance.
- NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_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." NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_provenance.
- NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_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." NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance.
- NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_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." NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_provenance.