Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_provenance.
- NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_assertion wasGeneratedBy ECO_0000203 NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_provenance.
- NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_assertion wasDerivedFrom befree-20140225 NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_provenance.
- NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_assertion SIO_000772 20234391 NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_provenance.
- NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_assertion evidence source_evidence_literature NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_provenance.
- NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_assertion description "[Dystroglycan is a protein which binds directly to two proteins defective in muscular dystrophies (dystrophin and laminin alpha2) and whose own aberrant post-translational modification is the common aetiological route of neuromuscular diseases associated with mutations in genes encoding at least six other proteins (POMT1, POMT2, POMGnT1, LARGE, FKTN and FKRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP447636.RADnvxmMam4s2TNEDxsQ9B4QAeqpLLzUG45kud2M8sHOk130_provenance.