Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_assertion> ?p ?o ?g. }
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- NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_assertion type Assertion NP682733.RAe3lJSXGQMSVBsyImrg4F8JQxAK5bdu6Z9wR-cEfiPA8130_head.
- 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.