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- source_evidence_literature type ECO_0000212 NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_provenance.
- NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_assertion description "[About 30% of the mutations causing nonsyndromic X-linked mental retardation (MRX) are thought to be located in Xp11 and in the pericentromeric region, with a particular clustering of gene defects in a 7.4 Mb interval flanked by the genes ELK1 and ALAS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_provenance.
- NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_assertion evidence source_evidence_literature NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_provenance.
- NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_assertion SIO_000772 16969374 NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_provenance.
- NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_assertion wasDerivedFrom befree-2016 NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_provenance.
- NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_assertion wasGeneratedBy ECO_0000203 NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_provenance.
- befree-2016 importedOn "2016-02-19" NP569088.RAwvg50mt_cae0R-nENXo7I6Geyg84LUapqhs1GEDw5T0130_provenance.