Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_provenance.
- NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_assertion description "[The authors compare neurologic and neuroradiologic follow-up data of six patients carrying TREM2 mutations with PLOSL due to defective DAP12 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_provenance.
- NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_assertion evidence source_evidence_literature NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_provenance.
- NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_assertion SIO_000772 15883308 NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_provenance.
- NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_assertion wasDerivedFrom befree-2016 NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_provenance.
- NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_assertion wasGeneratedBy ECO_0000203 NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_provenance.
- befree-2016 importedOn "2016-02-19" NP493964.RAgYHHwu_wUbLx2N5M-hE93uEJbtLLjaKqux6603wIvUc130_provenance.