Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_provenance.
- NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_assertion description "[Recently, it has been shown that genetic defects of human DAP12/KARAP and TREM-2 result in a rare syndrome characterized by bone cysts and presenile dementia called Nasu-Hakola disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_provenance.
- NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_assertion evidence source_evidence_literature NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_provenance.
- NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_assertion SIO_000772 12913093 NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_provenance.
- NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_assertion wasDerivedFrom befree-20140225 NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_provenance.
- NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_assertion wasGeneratedBy ECO_0000203 NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615390.RAtjnZp2wFMJHVRIcUIMLGoku1oBv40YH8n5Gfad6itF4130_provenance.