Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_provenance.
- NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_assertion description "[Z alpha-1 antitrypsin (AAT) deficiency is a genetic disease associated with accumulation of misfolded AAT in the endoplasmic reticulum (ER) of hepatocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_provenance.
- NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_assertion evidence source_evidence_curated NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_provenance.
- NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_assertion SIO_000772 17559149 NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_provenance.
- NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_assertion wasDerivedFrom ctd_human-20150221 NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_provenance.
- NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_assertion wasGeneratedBy ECO_0000218 NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP29384.RAGrFiIwDd5GVl3m3gnSJl3jr-_WwYxr0EOJ3JakqryTw130_provenance.