Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_assertion> ?p ?o ?g. }
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- NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_assertion type Assertion NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_head.
- NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_assertion description "[XLSA is due to mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_provenance.
- NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_assertion evidence source_evidence_curated NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_provenance.
- NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_assertion SIO_000772 21309041 NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_provenance.
- NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_assertion wasDerivedFrom uniprot-2016 NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_provenance.
- NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_assertion wasGeneratedBy ECO_0000218 NP6522.RAQ7nwz4KCB138TyxseLfAanBXkr8qh7LywYHJLrHGI8U130_provenance.