Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_provenance.
- NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_assertion description "[A single point mutation (Val617Phe) was identified in JAK2 in 71 (97%) of 73 patients with polycythaemia vera, 29 (57%) of 51 with essential thrombocythaemia, and eight (50%) of 16 with idiopathic myelofibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_provenance.
- NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_assertion evidence source_evidence_curated NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_provenance.
- NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_assertion SIO_000772 15781101 NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_provenance.
- NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_assertion wasDerivedFrom ctd_human-20130708 NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_provenance.
- NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_assertion wasGeneratedBy ECO_0000218 NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP20666.RA-wjXqFi28XcaGQiw4cCQz3VwEnMc615t3ncfgkzHmgc130_provenance.