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- source_evidence_literature type ECO_0000212 NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_provenance.
- NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_assertion description "[We recently identified mutations of ARX in nine genotypic males with X-linked lissencephaly with abnormal genitalia (XLAG), and in several female relatives with isolated agenesis of the corpus callosum (ACC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_provenance.
- NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_assertion evidence source_evidence_literature NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_provenance.
- NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_assertion SIO_000772 14722918 NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_provenance.
- NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_assertion wasDerivedFrom befree-2016 NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_provenance.
- NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_assertion wasGeneratedBy ECO_0000203 NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_provenance.
- befree-2016 importedOn "2016-02-19" NP427984.RAD3KFzSBYOSEdr0nFp_d_47wNsXrB1pDWhJEJWOx9y_E130_provenance.