Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_provenance.
- NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_assertion description "[The conditions studied were scans of genetically confirmed cases of Becker muscular dystrophy (BMD) (n = 28), LGMD2C-F (sarcoglycanopathies) (n = 11), LGMD2I (n = 4), LGMD1B (n = 26), LGMD2A (n = 24), Bethlem myopathy (n = 14), and LGMD2L (n = 11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_provenance.
- NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_assertion evidence source_evidence_literature NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_provenance.
- NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_assertion SIO_000772 23035061 NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_provenance.
- NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_assertion wasDerivedFrom befree-20140225 NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_provenance.
- NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_assertion wasGeneratedBy ECO_0000203 NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP531087.RAu1QykEnbtF6oFqrYc-In1IkJAO6jpkiV2k8Am0uM2Xo130_provenance.