Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_provenance.
- NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_assertion description "[Mutations in the genes encoding ATP7A and ATP7B lead to copper deficiency and toxicity disorders, Menkes and Wilson diseases, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_provenance.
- NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_assertion evidence source_evidence_literature NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_provenance.
- NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_assertion SIO_000772 21242307 NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_provenance.
- NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_assertion wasDerivedFrom befree-20140225 NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_provenance.
- NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_assertion wasGeneratedBy ECO_0000203 NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_provenance.