Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_assertion> ?p ?o ?g. }
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- NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_assertion type Assertion NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_head.
- NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_assertion description "[Mutations in the specific delta-aminolevulinic acid synthase (ALAS) 2 isoform that catalyses the first and rate-limiting step in heme synthesis pathway in the mitochondrial matrix, lead to ineffective erythropoiesis that characterizes X-linked sideroblastic anemia (XLSA), the most common inherited sideroblastic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_provenance.
- NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_assertion evidence source_evidence_curated NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_provenance.
- NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_assertion SIO_000772 16892088 NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_provenance.
- NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_assertion wasDerivedFrom ctd_human-20150221 NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_provenance.
- NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_assertion wasGeneratedBy ECO_0000218 NP6497.RAIAcqnzWXA49Jebx18FFXD6t01x0O9pP9Ykp2g0lTSTU130_provenance.