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- NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_assertion type Assertion NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_head.
- NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_assertion wasGeneratedBy ECO_0000203 NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_provenance.
- NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_assertion wasDerivedFrom befree-2016 NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_provenance.
- NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_assertion SIO_000772 15965158 NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_provenance.
- NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_assertion evidence source_evidence_literature NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_provenance.
- NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_assertion description "[The data indicate that the novel mutation 640C>T in the OA1 gene is the primary cause of the eye disease in the family studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500157.RA9w5Oy-4qPMsG5NY1H-8KU2n05zW3QVWJw3U65mMM9w4130_provenance.