Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_provenance.
- NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_assertion description "[The absence of del(5q), trisomy 8 and 21, as well as the rarity of monosomy 7, contrasts with pooled published data and may reflect our exclusion of closely related disorders, in particular MDS with fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_provenance.
- NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_assertion evidence source_evidence_literature NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_provenance.
- NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_assertion SIO_000772 7819070 NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_provenance.
- NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_assertion wasDerivedFrom befree-20140225 NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_provenance.
- NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_assertion wasGeneratedBy ECO_0000203 NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP519422.RAlTdrwhgIBfH6oNHt9wZTdEJkLMKmWwgBDK_1k38X_aM130_provenance.