Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_provenance.
- NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_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." NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_provenance.
- NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_assertion evidence source_evidence_literature NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_provenance.
- NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_assertion SIO_000772 12913093 NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_provenance.
- NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_assertion wasDerivedFrom befree-20140225 NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_provenance.
- NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_assertion wasGeneratedBy ECO_0000203 NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP589262.RAAZZI3XQi0kbFULNiA1WvB_w6IJiEWb1gsX6L02CcXaw130_provenance.