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- source_evidence_literature type ECO_0000212 NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_provenance.
- NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_assertion wasGeneratedBy ECO_0000203 NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_provenance.
- NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_assertion wasDerivedFrom befree-20150227 NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_provenance.
- NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_assertion SIO_000772 23543484 NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_provenance.
- NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_assertion evidence source_evidence_literature NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_provenance.
- NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_assertion description "[Our results demonstrate that the TNPO3 mutation is the cause of limb-girdle muscular dystrophy 1F, expand our knowledge of the molecular basis of muscular dystrophies and bolster the importance of defects of nuclear envelope proteins as causes of inherited myopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874644.RAqvg0CHCeBH5smcVeonnYho-grQYXa57pMy-6FJArFrQ130_provenance.