Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_provenance.
- NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_assertion description "[Mutations in TET2, RUNX1 and JAK2(V617F) are involved in myelodysplastic and/or myeloproliferative syndromes, and more specifically in CMML but were not found in JMML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_provenance.
- NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_assertion evidence source_evidence_literature NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_provenance.
- NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_assertion SIO_000772 20955399 NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_provenance.
- NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_assertion wasDerivedFrom befree-20140225 NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_provenance.
- NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_assertion wasGeneratedBy ECO_0000203 NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP352485.RA_s2mt59sszo0HKZNcR-vlN8jtiNRO44U-E1mjCXCMyA130_provenance.