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- NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_assertion type Assertion NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_head.
- NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_assertion wasGeneratedBy ECO_0000203 NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_provenance.
- NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_assertion wasDerivedFrom befree-20150227 NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_provenance.
- NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_assertion SIO_000772 1979048 NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_provenance.
- NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_assertion evidence source_evidence_literature NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_provenance.
- NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_assertion description "[Two independent familial STS deletions, one of which is associated with a phenotype of ichthyosis plus ocular albinism (XI/OA1) and the other with nystagmus plus Rud syndrome, lack some but not all of the normal S232 PFGE fragments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252997.RAuEB5bov73uT3wlwB-53OD-qtuKNNu_1f2JEOs020COU130_provenance.