Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_provenance.
- NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_assertion description "[APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_provenance.
- NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_assertion evidence source_evidence_literature NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_provenance.
- NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_assertion SIO_000772 1679288 NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_provenance.
- NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_assertion wasDerivedFrom befree-20150227 NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_provenance.
- NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_assertion wasGeneratedBy ECO_0000203 NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP867707.RAxyA-VMXlb8DnvQYhpT3R5d3t8xscIapKJzbSyF4KI3w130_provenance.