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- source_evidence_literature type ECO_0000212 NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_provenance.
- NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_assertion description "[We have studied the mutational status of TET2 (complete coding region), ASXL1 (exon12), IDH1 (R132), IDH2 (R140 and R172), and c-CBL (exons 8 and 9) in 62 MPN patients (52 essential thrombocythemia (ET), five polycythemia vera (PV), and five primary myelofibrosis (PMF)) negative for both JAK2 (V617F and exon 12) and MPL (exon 10) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_provenance.
- NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_assertion evidence source_evidence_literature NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_provenance.
- NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_assertion SIO_000772 21904853 NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_provenance.
- NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_assertion wasDerivedFrom befree-20150227 NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_provenance.
- NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_assertion wasGeneratedBy ECO_0000203 NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP475353.RA3-S7XBN6AMyrvWAMpV7JrXhLC3G0KxDXNk_QqfJSbdw130_provenance.