Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_provenance.
- NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_assertion description "[These data indicate that a lack of FMRP leads to cerebellar deficits at both the cellular and behavioral levels and raise the possibility that cerebellar dysfunctions can contribute to motor learning deficits in Fragile X patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_provenance.
- NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_assertion evidence source_evidence_literature NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_provenance.
- NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_assertion SIO_000772 16055059 NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_provenance.
- NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_assertion wasDerivedFrom befree-2016 NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_provenance.
- NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_assertion wasGeneratedBy ECO_0000203 NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_provenance.
- befree-2016 importedOn "2016-02-19" NP506564.RAGnx01yOozo1qlyn4kk7ium10k9gf_kgYUeT50p3XQdM130_provenance.