Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_provenance.
- NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_assertion description "[Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_provenance.
- NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_assertion evidence source_evidence_curated NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_provenance.
- NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_assertion SIO_000772 20697050 NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_provenance.
- NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_assertion wasDerivedFrom uniprot-2016 NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_provenance.
- NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_assertion wasGeneratedBy ECO_0000218 NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6319.RA2j7p7DFX8xB8902oJdkyMgr_rdBtuK3VuOByFJFwBis130_provenance.