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- NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_assertion type Assertion NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_head.
- NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_assertion wasGeneratedBy ECO_0000203 NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_provenance.
- NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_assertion wasDerivedFrom befree-20140225 NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_provenance.
- NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_assertion SIO_000772 16724007 NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_provenance.
- NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_assertion evidence source_evidence_literature NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_provenance.
- NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_assertion description "[Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP909419.RADm3iSrZBEQ_ctdKW96QJO-ItnXAipOD5scLfL-ayutM130_provenance.