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- source_evidence_literature type ECO_0000212 NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_provenance.
- befree-2016 importedOn "2016-02-19" NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_provenance.
- NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_assertion wasGeneratedBy ECO_0000203 NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_provenance.
- NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_assertion wasDerivedFrom befree-2016 NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_provenance.
- NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_assertion SIO_000772 20234391 NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_provenance.
- NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_assertion evidence source_evidence_literature NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_provenance.
- NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_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." NP800435.RALO1ahBXineuO1w955XIMfI2r1RNF1Zn3lvgcgA3WUV4130_provenance.