Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_provenance.
- NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_assertion description "[Complex karyotypes are seen in approximately 15% of de novo MDS/AML and in up to 50% of therapy-related MDS/AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_provenance.
- NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_assertion evidence source_evidence_literature NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_provenance.
- NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_assertion SIO_000772 16142824 NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_provenance.
- NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_assertion wasDerivedFrom befree-20150227 NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_provenance.
- NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_assertion wasGeneratedBy ECO_0000203 NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP606157.RAQ4yc5nC76Fu7v8l9Nw_uHGN_rqpud43hEnQHl0zRsYQ130_provenance.