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- NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_assertion type Assertion NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_head.
- NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_provenance.
- NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_assertion evidence source_evidence_literature NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_provenance.
- NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_assertion SIO_000772 19131948 NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_provenance.
- NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_assertion wasDerivedFrom befree-2016 NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_provenance.
- NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_assertion wasGeneratedBy ECO_0000203 NP713084.RA2x6zS8Df5kp7dGX5lOsBpR-_dS6-jSNXBOjT_RLt7fw130_provenance.