Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance.
- NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_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." NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance.
- NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_assertion evidence source_evidence_literature NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance.
- NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_assertion SIO_000772 12928484 NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance.
- NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_assertion wasDerivedFrom befree-2016 NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance.
- NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_assertion wasGeneratedBy ECO_0000203 NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance.
- befree-2016 importedOn "2016-02-19" NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance.