Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_assertion> ?p ?o ?g. }
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- NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_assertion type Assertion NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_head.
- NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_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." NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_provenance.
- NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_assertion evidence source_evidence_literature NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_provenance.
- NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_assertion SIO_000772 21242307 NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_provenance.
- NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_assertion wasDerivedFrom befree-2016 NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_provenance.
- NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_assertion wasGeneratedBy ECO_0000203 NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_provenance.