Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_assertion> ?p ?o ?g. }
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- NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_assertion type Assertion NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_head.
- NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_assertion description "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_provenance.
- NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_assertion evidence source_evidence_curated NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_provenance.
- NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_assertion SIO_000772 12928484 NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_provenance.
- NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_assertion wasDerivedFrom uniprot-20130724 NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_provenance.
- NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_assertion wasGeneratedBy ECO_0000218 NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_provenance.