Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_provenance.
- befree-2016 importedOn "2016-02-19" NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_provenance.
- NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_assertion wasGeneratedBy ECO_0000203 NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_provenance.
- NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_assertion wasDerivedFrom befree-2016 NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_provenance.
- NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_assertion SIO_000772 16987873 NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_provenance.
- NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_assertion evidence source_evidence_literature NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_provenance.
- NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_assertion description "[The finding of a significant number of copy number polymorphisms in the genome in the normal population, means that assigning pathogenicity to deletions and duplications in patients with mental retardation can be difficult but has been identified for duplications of MECP2 and L1CAM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570295.RArewTnoqLjPwelvNcrTvWK2KshoHNy2xVq1Guq5kXw7c130_provenance.