Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_provenance.
- NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_assertion wasGeneratedBy ECO_0000203 NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_provenance.
- NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_assertion wasDerivedFrom befree-20140225 NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_provenance.
- NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_assertion SIO_000772 22468107 NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_provenance.
- NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_assertion evidence source_evidence_literature NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_provenance.
- NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_assertion description "[The patients with dysferlinopathy were classified by initial muscle weakness: fifteen patients with Miyoshi myopathy phenotype (MM), thirteen patients with limb girdle muscular dystrophy 2B phenotype (LGMD2B), two patients with proximodistal phenotype, and one asymptomatic patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401352.RABius6xTYsmZ0DR8wNIr-vMTdbYr6rCAAhL9spHEjLe8130_provenance.