Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_provenance.
- NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_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." NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_provenance.
- NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_assertion evidence source_evidence_literature NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_provenance.
- NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_assertion SIO_000772 16055059 NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_provenance.
- NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_assertion wasDerivedFrom befree-20140225 NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_provenance.
- NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_assertion wasGeneratedBy ECO_0000203 NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718904.RAx5a88YqzVW94wNSalmIeEvx2mPNfYJoeccaIeMX_zbM130_provenance.