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- source_evidence_literature type ECO_0000212 NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_provenance.
- NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_assertion description "[Mutations in the Aristaless related homeobox (ARX) gene are associated with a broad spectrum of disorders, including nonsyndromic X-linked mental retardation, sometimes associated with epilepsy, as well as syndromic forms with brain abnormalities and abnormal genitalia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_provenance.
- NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_assertion evidence source_evidence_literature NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_provenance.
- NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_assertion SIO_000772 17044103 NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_provenance.
- NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_assertion wasDerivedFrom befree-20150227 NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_provenance.
- NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_assertion wasGeneratedBy ECO_0000203 NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978186.RAJCXWQx5uyF9nic4DQYwLP2CfR8GAyf6wyjxQD8_zbBo130_provenance.