Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_provenance.
- NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_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." NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_provenance.
- NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_assertion evidence source_evidence_literature NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_provenance.
- NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_assertion SIO_000772 21426321 NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_provenance.
- NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_assertion wasDerivedFrom befree-2016 NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_provenance.
- NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_assertion wasGeneratedBy ECO_0000203 NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_provenance.
- befree-2016 importedOn "2016-02-19" NP881486.RAMEawc-VGvVwBrF3U0xZcYmB0TDXfE75K1M9W_jy_NbY130_provenance.