Matches in Nanopublications for { ?s ?p "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance.
- NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance.
- NP402803.RA8f3Ca32VRK330C-A-7MN96y8h0-zQSGOIo5MLQRExSM130_assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402803.RA8f3Ca32VRK330C-A-7MN96y8h0-zQSGOIo5MLQRExSM130_provenance.
- assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP322913.RAAz-SB9h_q-5CAg_LmdUgEJJ1qjn1ykQMzeSVibEWUUA130_assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322913.RAAz-SB9h_q-5CAg_LmdUgEJJ1qjn1ykQMzeSVibEWUUA130_provenance.
- NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322918.RAQD2N4b8Fcbo-L8VhpKZZTWK9kOFvt-MIy0xDds6gHYI130_provenance.
- NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616270.RAn1BzXM0Fi1GPo9TwTaG1qcfla_GakX8NWXVH3ODcccY130_provenance.
- NP985435.RAIvnQm5tqJzq0-gBJP6NDE4lxrLB3ewDey3C7Bhu1OsU130_assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985435.RAIvnQm5tqJzq0-gBJP6NDE4lxrLB3ewDey3C7Bhu1OsU130_provenance.
- NP1504.RAE4Z-NVLcHJKzv1_NO3a5gTusuHzxHXd8pd5jbp9mzUc130_assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1504.RAE4Z-NVLcHJKzv1_NO3a5gTusuHzxHXd8pd5jbp9mzUc130_provenance.