Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_provenance.
- NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_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." NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_provenance.
- NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_assertion evidence source_evidence_literature NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_provenance.
- NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_assertion SIO_000772 8782832 NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_provenance.
- NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_assertion wasDerivedFrom befree-2016 NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_provenance.
- NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_assertion wasGeneratedBy ECO_0000203 NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1356561.RAEzB61L1wSeVqfRIc76vTflIP0D1C6BOlIOlQpbq-hKI130_provenance.