Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_provenance.
- NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_assertion description "[Severe erythrocyte adenylate kinase deficiency due to homozygous A-->G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_provenance.
- NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_assertion evidence source_evidence_curated NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_provenance.
- NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_assertion SIO_000772 9432020 NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_provenance.
- NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_assertion wasDerivedFrom uniprot-2016 NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_provenance.
- NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_assertion wasGeneratedBy ECO_0000218 NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9586.RACa4NFOVFd_3ts5Gcds55JjPbHVtL9ZsW7Yovq5SNt-4130_provenance.