Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_provenance.
- befree-2016 importedOn "2016-02-19" NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_provenance.
- NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_assertion wasGeneratedBy ECO_0000203 NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_provenance.
- NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_assertion wasDerivedFrom befree-2016 NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_provenance.
- NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_assertion SIO_000772 12467726 NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_provenance.
- NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_assertion evidence source_evidence_literature NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_provenance.
- NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_assertion description "[These cases, in addition to those reported previously, confirmed the large phenotypic variability in the group of secondary merosin deficiency congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376645.RAXc09MMFXfozKw-QJxHAr5fqOz1TUsYZRgSzHcNnCfHY130_provenance.