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- source_evidence_literature type ECO_0000212 NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_provenance.
- NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_assertion description "[DYSF encoding dysferlin is mutated in Miyoshi myopathy and Limb-Girdle Muscular Dystrophy type 2B, the two main phenotypes recognized in dysferlinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_provenance.
- NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_assertion evidence source_evidence_literature NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_provenance.
- NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_assertion SIO_000772 16010686 NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_provenance.
- NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_assertion wasDerivedFrom befree-2016 NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_provenance.
- NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_assertion wasGeneratedBy ECO_0000203 NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_provenance.
- befree-2016 importedOn "2016-02-19" NP503633.RA1y_-qTK8wCxvMVAncxyDqBThK9lhQbK22-4tpfanfRY130_provenance.