Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_provenance.
- NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_assertion description "[The more common X-linked recessive form of EDMD is caused by mutations in either EMD (encoding emerin) or FHL1 (encoding four and a half LIM domains 1), while mutations in LMNA (encoding lamin A/C), SYNE1 (encoding nesprin-1) and SYNE2 (encoding nesprin-2) lead to autosomal dominant forms of the condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_provenance.
- NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_assertion evidence source_evidence_literature NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_provenance.
- NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_assertion SIO_000772 23456229 NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_provenance.
- NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_assertion wasDerivedFrom befree-20140225 NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_provenance.
- NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_assertion wasGeneratedBy ECO_0000203 NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP159957.RAhF90DYI4e8KN0254nErrEFz983mWZoMROUEQj1dP_uo130_provenance.