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- source_evidence_literature type ECO_0000212 NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_provenance.
- NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_assertion description "[Polyalanine (polyA)-expansion-encoding mutations of aristaless-related homeobox (ARX) cause a spectrum of X-linked ID (XLID) diseases and chronic epilepsy, including infantile spasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_provenance.
- NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_assertion evidence source_evidence_literature NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_provenance.
- NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_assertion SIO_000772 23246292 NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_provenance.
- NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_assertion wasDerivedFrom befree-20150227 NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_provenance.
- NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_assertion wasGeneratedBy ECO_0000203 NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978129.RAKgAyVVMhEG7wAjJ5ako51k31YU7ywAwLePtmk5Qf_X0130_provenance.