Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_provenance.
- NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_assertion description "[Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_provenance.
- NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_assertion evidence source_evidence_literature NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_provenance.
- NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_assertion SIO_000772 21209411 NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_provenance.
- NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_assertion wasDerivedFrom befree-2016 NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_provenance.
- NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_assertion wasGeneratedBy ECO_0000203 NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_provenance.
- befree-2016 importedOn "2016-02-19" NP863395.RARN37avRZlTTh29rF9IxAdhSMoOHFgc96iFIGec3oC8U130_provenance.