Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_provenance.
- NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_assertion wasGeneratedBy ECO_0000203 NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_provenance.
- NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_assertion wasDerivedFrom befree-20140225 NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_provenance.
- NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_assertion SIO_000772 22549409 NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_provenance.
- NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_assertion evidence source_evidence_literature NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_provenance.
- NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_assertion description "[Clinical phenotype in POMT1-mutated patients ranges from congenital muscular dystrophy (CMD) with structural brain abnormalities, to limb-girdle muscular dystrophy (LGMD) with microcephaly and mental retardation, to mild LGMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP383941.RAAR8Zkabbqm0SkIjXEoYGCQ0fYKakSVKCGwHV_1PV8wg130_provenance.