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- source_evidence_literature type ECO_0000212 NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_provenance.
- NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_assertion description "[Fragile X syndrome with FMR1 and FMR2 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_provenance.
- NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_assertion evidence source_evidence_literature NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_provenance.
- NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_assertion SIO_000772 10424820 NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_provenance.
- NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_assertion wasDerivedFrom befree-20150227 NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_provenance.
- NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_assertion wasGeneratedBy ECO_0000203 NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP409169.RA9YCMlmuwCu6eudcqlaMduXQLFHlDSP6S3pU-fziqsAk130_provenance.