Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_provenance.
- NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_assertion description "[The relatively low observed frequency of MECP2 mutations reflects a wide spectrum of mental disability disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_provenance.
- NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_assertion evidence source_evidence_literature NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_provenance.
- NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_assertion SIO_000772 19652677 NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_provenance.
- NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_assertion wasDerivedFrom befree-20140225 NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_provenance.
- NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_assertion wasGeneratedBy ECO_0000203 NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP837025.RAiG3L1dKkXb4q2Yyi1Dsb2Bfg4eGW_g0184VDnn22yVQ130_provenance.