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- source_evidence_literature type ECO_0000212 NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_provenance.
- NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_assertion description "[A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_provenance.
- NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_assertion evidence source_evidence_literature NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_provenance.
- NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_assertion SIO_000772 21426321 NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_provenance.
- NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_assertion wasDerivedFrom befree-20150227 NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_provenance.
- NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_assertion wasGeneratedBy ECO_0000203 NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978146.RA9gTQqtYg0-ii4p37Iv_t8pLblw-EI_36wrAxp72r8I8130_provenance.