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- source_evidence_literature type ECO_0000212 NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_provenance.
- NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_assertion description "[Altogether eight abnormalities were repeatedly identified both as sole chromosomal anomalies and as part of more complex karyotypes: the structural rearrangements i(1)(q10), der(1:16)(q10;p10), del(1)(q11-12), del(3)(p12-13p14-21), and del(6)(q21-22) and the numerical aberrations +7, +18, and +20.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_provenance.
- NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_assertion evidence source_evidence_literature NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_provenance.
- NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_assertion SIO_000772 7536456 NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_provenance.
- NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_assertion wasDerivedFrom befree-2016 NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_provenance.
- NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_assertion wasGeneratedBy ECO_0000203 NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1311292.RAnrF5NHudpEduBuqSCHtDf93rbXQM941qNzhqlX5WkrA130_provenance.