Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_provenance.
- NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_assertion description "[Duchenne (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive disorders, caused by mutations in the dystrophin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_provenance.
- NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_assertion evidence source_evidence_literature NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_provenance.
- NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_assertion SIO_000772 20847377 NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_provenance.
- NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_assertion wasDerivedFrom gad-20130706 NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_provenance.
- NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_assertion wasGeneratedBy ECO_0000203 NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_provenance.
- gad-20130706 importedOn "2013-07-06" NP60192.RAQI0wHnW32zHrgewK0jRwV0UnyIrI-q_2BPWeNGUBaBs130_provenance.