Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_provenance.
- NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_assertion description "[In this article, we identify a gene, SLC39A4, located in the candidate region and, in patients with AE, document mutations that likely lead to the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_provenance.
- NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_assertion evidence source_evidence_curated NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_provenance.
- NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_assertion SIO_000772 12032886 NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_provenance.
- NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_assertion wasDerivedFrom uniprot-20130724 NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_provenance.
- NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_assertion wasGeneratedBy ECO_0000218 NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6140.RAwVCUeR3t_sUEXXwqnYUtvlMDUJGjGGsi1dNpcdbbQrY130_provenance.