Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_provenance.
- NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_assertion description "[In addition to the results demonstrating the involvement of MECP2 in MRX, this study shows that the frequency of mutations in MECP2 in the mentally retarded population screened for the fragile X syndrome is comparable to the frequency of the CGG expansions in FMR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_provenance.
- NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_assertion evidence source_evidence_literature NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_provenance.
- NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_assertion SIO_000772 11309367 NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_provenance.
- NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_assertion wasDerivedFrom befree-2016 NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_provenance.
- NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_assertion wasGeneratedBy ECO_0000203 NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_provenance.
- befree-2016 importedOn "2016-02-19" NP314939.RAO-WbgNSaFcR5LzhK7bGKE1w5pUAW_oriLZvljqz8FDs130_provenance.