Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_provenance.
- NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_assertion description "[Generation of the NUP98-HOXD13 fusion transcript by a rare translocation, t(2;11)(q31;p15), in a case of infant leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_provenance.
- NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_assertion evidence source_evidence_literature NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_provenance.
- NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_assertion SIO_000772 10931000 NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_provenance.
- NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_assertion wasDerivedFrom befree-2016 NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_provenance.
- NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_assertion wasGeneratedBy ECO_0000203 NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_provenance.
- befree-2016 importedOn "2016-02-19" NP291129.RAZTVXDgPry8neMN5Fn4GLN-bcebGf2uwf0u9gQMKSsSM130_provenance.