Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance.
- NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_assertion description "[Following the recent discovery that the methyl-CpG binding protein 2 (MECP2) gene located on Xq28 is involved in Rett syndrome (RTT), a wild spectrum of phenotypes, including mental handicap, has been shown to be associated with mutations in MECP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance.
- NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_assertion evidence source_evidence_literature NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance.
- NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_assertion SIO_000772 11309367 NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance.
- NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_assertion wasDerivedFrom befree-20140225 NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance.
- NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_assertion wasGeneratedBy ECO_0000203 NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP912095.RA91Twor7aZNzm2BUkqOZvOpTyfp0QFpnomoAez6tMTSo130_provenance.