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- source_evidence_literature type ECO_0000212 NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_provenance.
- NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_assertion description "[study underlines the role of ARXdup24 as a critical mutational site causing mental retardation linked to Xp22 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_provenance.
- NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_assertion evidence source_evidence_literature NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_provenance.
- NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_assertion SIO_000772 17480217 NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_provenance.
- NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_assertion wasDerivedFrom lhgdn-20090331 NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_provenance.
- NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_assertion wasGeneratedBy ECO_0000203 NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP224917.RAxonqw1puombV2iedjcswe_sMELKVIvgwweJNTjtPfVg130_provenance.