Matches in Nanopublications for { ?s ?p "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance.
- NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378761.RA8MOHbKnOsxgZnWzrOKnKvRNPsEhl1MIePP9REEpuIVQ130_provenance.
- assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP356715.RAbcTyflOj8DWhWvu9Uz9k4oydiqEwjY_gRgib1Kk26g4130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356715.RAbcTyflOj8DWhWvu9Uz9k4oydiqEwjY_gRgib1Kk26g4130_provenance.
- NP815617.RA_-miElO8Zk_A3uq7fm--LV0Hr7MQ_nCTpuDnaXxw1y4130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815617.RA_-miElO8Zk_A3uq7fm--LV0Hr7MQ_nCTpuDnaXxw1y4130_provenance.
- assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP789945.RABukzX_YTkqXQ8WsTqJGspkpdZaZwaDdo5mxis64nmxA130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789945.RABukzX_YTkqXQ8WsTqJGspkpdZaZwaDdo5mxis64nmxA130_provenance.
- NP322915.RAB3iiOtcDYlYIV0cu4HhK7CYkWpaXQTONVKhTVqnrvzE130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322915.RAB3iiOtcDYlYIV0cu4HhK7CYkWpaXQTONVKhTVqnrvzE130_provenance.
- NP322914.RAiOqtxSi5GEgwwizBuyz3wNb5nvimYhMD4n98NWxZ5rE130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322914.RAiOqtxSi5GEgwwizBuyz3wNb5nvimYhMD4n98NWxZ5rE130_provenance.
- NP247110.RAMq_mizh46WCa-vuqk-JOYKFpErhpQiWw6UT008Lg0rs130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247110.RAMq_mizh46WCa-vuqk-JOYKFpErhpQiWw6UT008Lg0rs130_provenance.
- NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322916.RAEQwOO-SHZQNjxouv2uMt6yfeSLiqvT-Z4-js2Z7tz4c130_provenance.
- NP322917.RAPr9kOUMtd9F2KXkE6mwij1qDm4NnR7SXHZS9XjX16qI130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322917.RAPr9kOUMtd9F2KXkE6mwij1qDm4NnR7SXHZS9XjX16qI130_provenance.
- NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_provenance.