Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance.
- NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_assertion wasGeneratedBy ECO_0000203 NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance.
- NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_assertion wasDerivedFrom befree-20150227 NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance.
- NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_assertion SIO_000772 11749051 NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance.
- NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_assertion evidence source_evidence_literature NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance.
- NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_assertion description "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835151.RAWU2U95_Gq8LTjGwqjlfs2E4zrewU-PKQKEcxlqFvxwk130_provenance.