Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_provenance.
- NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_assertion description "[FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_provenance.
- NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_assertion evidence source_evidence_literature NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_provenance.
- NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_assertion SIO_000772 20858599 NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_provenance.
- NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_assertion wasDerivedFrom befree-20140225 NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_provenance.
- NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_assertion wasGeneratedBy ECO_0000203 NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP849805.RAjjOgjULTU5F5kQobW64r6GmZ7DA0nWNLtZAJYCQfqzw130_provenance.