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- source_evidence_literature type ECO_0000212 NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_provenance.
- NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_assertion description "[Mutations in the Aristaless-related homeobox (ARX) gene are associated with a broad spectrum of disorders including X-linked lissencephaly with abnormal genitalia (XLAG) and absent corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_provenance.
- NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_assertion evidence source_evidence_literature NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_provenance.
- NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_assertion SIO_000772 15248097 NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_provenance.
- NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_assertion wasDerivedFrom befree-20150227 NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_provenance.
- NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_assertion wasGeneratedBy ECO_0000203 NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978133.RAqjY88xQyzk5Jrt3Uw3EjjpuawmmVNDn1NYyjtNU7-Rk130_provenance.