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- source_evidence_literature type ECO_0000212 NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_provenance.
- NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_assertion description "[Our findings highlight the importance of a molecular diagnosis in CMS and demonstrate considerable similarities between patients with MUSK and DOK7-related CMS in terms of clinical phenotype and treatment options.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_provenance.
- NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_assertion evidence source_evidence_literature NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_provenance.
- NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_assertion SIO_000772 24183479 NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_provenance.
- NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_assertion wasDerivedFrom befree-20150227 NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_provenance.
- NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_assertion wasGeneratedBy ECO_0000203 NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP984591.RAJeqbhWC9BHYt-aWLax3fPjZVyWICcErbvRt7MU-x3_s130_provenance.