Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance.
- NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_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." NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance.
- NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_assertion evidence source_evidence_literature NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance.
- NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_assertion SIO_000772 21496628 NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance.
- NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_assertion wasDerivedFrom befree-2016 NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance.
- NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_assertion wasGeneratedBy ECO_0000203 NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance.
- befree-2016 importedOn "2016-02-19" NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance.