Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_provenance.
- NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_assertion wasGeneratedBy ECO_0000203 NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_provenance.
- NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_assertion wasDerivedFrom befree-20150227 NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_provenance.
- NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_assertion SIO_000772 17442773 NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_provenance.
- NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_assertion evidence source_evidence_literature NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_provenance.
- NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_assertion description "[Analysis of NUP98 allelic expression in AML and myelodysplastic syndrome showed loss of heterozygosity observed in 29% of the former and 8% of the latter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601116.RABS7m7P-wSV7q16x3XEB-HHpdVRLsnAiYjYzx6rJ--1g130_provenance.