Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_assertion> ?p ?o ?g. }
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- NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_assertion type Assertion NP985662.RAXa_kwIONAp6MdFLLF1-PICgd_g0X6ooFmrlRfhsMl_o130_head.
- 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.