Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance.
- NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_assertion wasGeneratedBy ECO_0000203 NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance.
- NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_assertion wasDerivedFrom befree-20140225 NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance.
- NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_assertion SIO_000772 10341296 NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance.
- NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_assertion evidence source_evidence_literature NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance.
- NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP483578.RAJbrjIROy2tcHp4oHIJniC74tr2mDagA8g0Az0PRvhFY130_provenance.