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- source_evidence_literature type ECO_0000212 NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_provenance.
- NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_provenance.
- NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_assertion evidence source_evidence_literature NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_provenance.
- NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_assertion SIO_000772 10424820 NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_provenance.
- NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_assertion wasDerivedFrom befree-2016 NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_provenance.
- NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_assertion wasGeneratedBy ECO_0000203 NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_provenance.