Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_provenance.
- NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_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." NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_provenance.
- NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_assertion evidence source_evidence_literature NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_provenance.
- NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_assertion SIO_000772 16969374 NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_provenance.
- NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_assertion wasDerivedFrom befree-20140225 NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_provenance.
- NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_assertion wasGeneratedBy ECO_0000203 NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP505988.RArPa1SUPSMkan-xGm_zPwli_1Ebm4aH5xG5zYDTeOSMg130_provenance.