Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_provenance.
- NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_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." NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_provenance.
- NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_assertion evidence source_evidence_literature NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_provenance.
- NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_assertion SIO_000772 12913093 NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_provenance.
- NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_assertion wasDerivedFrom befree-2016 NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_provenance.
- NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_assertion wasGeneratedBy ECO_0000203 NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_provenance.
- befree-2016 importedOn "2016-02-19" NP405192.RAG-IKgl3xXcUVl0IpneTYM7IyM1kVWnmpoZd69QiPPxg130_provenance.