Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_provenance.
- NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_assertion description "[Mutations in the human aristaless-related homeobox (ARX) gene are amongst the major causes of developmental and neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_provenance.
- NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_assertion evidence source_evidence_literature NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_provenance.
- NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_assertion SIO_000772 22642246 NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_provenance.
- NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_assertion wasDerivedFrom befree-2016 NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_provenance.
- NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_assertion wasGeneratedBy ECO_0000203 NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_provenance.
- befree-2016 importedOn "2016-02-19" NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_provenance.