Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_provenance.
- NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_assertion description "[8p11 myeloproliferative syndrome (EMS) is a hematopoietic stem cell disorder characterized by myeloid hyperplasia and non-Hodgkin's lymphoma with chromosomal translocations fusing several genes, most commonly ZNF198, to fibroblast growth factor receptor-1 (FGFR1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_provenance.
- NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_assertion evidence source_evidence_literature NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_provenance.
- NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_assertion SIO_000772 15050920 NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_provenance.
- NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_assertion wasDerivedFrom befree-2016 NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_provenance.
- NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_assertion wasGeneratedBy ECO_0000203 NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_provenance.
- befree-2016 importedOn "2016-02-19" NP437604.RA7SLxDzlY8OV7lYYzGQ-NnVhzr31kGt78r5CV06nxY_w130_provenance.