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- source_evidence_literature type ECO_0000212 NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_provenance.
- NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_assertion description "[Given that this is a minimum incidence because complete inventory was not possible, this study of patients with Rett syndrome reinforces the fact that the great majority of patients with Rett syndrome have a MECP2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_provenance.
- NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_assertion evidence source_evidence_literature NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_provenance.
- NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_assertion SIO_000772 16647997 NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_provenance.
- NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_assertion wasDerivedFrom befree-2016 NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_provenance.
- NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_assertion wasGeneratedBy ECO_0000203 NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_provenance.
- befree-2016 importedOn "2016-02-19" NP547495.RA3QWRfdBSoH2TirCTjq7ckGAtx_TwVdd4t5hi6ifCgEE130_provenance.