Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance.
- NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance.
- NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_assertion evidence source_evidence_literature NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance.
- NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_assertion SIO_000772 21496628 NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance.
- NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_assertion wasDerivedFrom befree-20140225 NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance.
- NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_assertion wasGeneratedBy ECO_0000203 NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance.