Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_provenance.
- NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_assertion description "[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." NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_provenance.
- NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_assertion evidence source_evidence_literature NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_provenance.
- NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_assertion SIO_000772 16055059 NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_provenance.
- NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_assertion wasDerivedFrom lhgdn-20090331 NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_provenance.
- NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_assertion wasGeneratedBy ECO_0000203 NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP142226.RANzh811AkpbKObGmo32C58lKTXHufi98LXcxpcZ_4XxY130_provenance.