Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP865877.RAAjcfIbWTNrBSEDHoDK_K4PtdUyTFjzxHEgP6qOEbwV4130_provenance.