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- NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_assertion type Assertion NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_head.
- NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_assertion description "[Xp22.3 deletion in males can be associated with short stature (SHOX), chondrodysplasia punctata (ARSE), mental retardation (MRX49 locus), ichthyosis (STS), Kallmann syndrome (KAL1) and ocular albinism (OA1), according to the size of the deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_provenance.
- NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_assertion evidence source_evidence_literature NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_provenance.
- NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_assertion SIO_000772 18194880 NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_provenance.
- NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_assertion wasDerivedFrom befree-20150227 NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_provenance.
- NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_assertion wasGeneratedBy ECO_0000203 NP569574.RAT8o8y30Nd5Cac_bxGNO1_tL2moLD0TrrrsNnFLOw_MQ130_provenance.