Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance.
- NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance.
- NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_assertion evidence source_evidence_literature NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance.
- NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_assertion SIO_000772 17223983 NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance.
- NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_assertion wasDerivedFrom befree-2016 NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance.
- NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_assertion wasGeneratedBy ECO_0000203 NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance.
- befree-2016 importedOn "2016-02-19" NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance.