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- NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_assertion type Assertion NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_head.
- NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_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." NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_provenance.
- NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_assertion evidence source_evidence_curated NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_provenance.
- NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_assertion SIO_000772 19131948 NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_provenance.
- NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_assertion wasDerivedFrom uniprot-20150221 NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_provenance.
- NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_assertion wasGeneratedBy ECO_0000218 NP4595.RAQ67bFspmCjaHnNi3zJuC7OnklA3j5LltuWHXygcEObo130_provenance.