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- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion type Assertion NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_head.
- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_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." NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion evidence source_evidence_literature NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion SIO_000772 19131948 NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion wasDerivedFrom befree-20150227 NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion wasGeneratedBy ECO_0000203 NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.