Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_provenance.
- NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_assertion description "[Analogous to the putative perturbation of the anchoring function of the dystrophin-associated complex in congenital muscular dystrophy with mutations in the alpha 2-subunit of laminin, our observations suggest a similar mechanism in Bethlem myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_provenance.
- NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_assertion evidence source_evidence_literature NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_provenance.
- NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_assertion SIO_000772 8782832 NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_provenance.
- NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_assertion wasDerivedFrom befree-20140225 NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_provenance.
- NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_assertion wasGeneratedBy ECO_0000203 NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP430233.RA0tJKQDXYx2CUWDq8b6oEZ3dIId2zph56lNeDq1bM_G0130_provenance.