Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_provenance.
- NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_assertion description "[FHL1 mutations cause Emery-Dreifuss muscular dystrophy (OMIM 310300), X-linked myopathy with postural muscle atrophy (XMPMA, OMIM 300696), scapuloperoneal myopathy (OMIM 300695), or reducing body myopathy (OMIM 300717, 300718).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_provenance.
- NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_assertion evidence source_evidence_literature NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_provenance.
- NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_assertion SIO_000772 21932316 NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_provenance.
- NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_assertion wasDerivedFrom befree-2016 NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_provenance.
- NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_assertion wasGeneratedBy ECO_0000203 NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_provenance.
- befree-2016 importedOn "2016-02-19" NP924999.RAwBUBgYexfFU0N_PmY6ggY68KPhkeGLSixsf_PkteuLo130_provenance.