Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion> ?p ?o ?g. }
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- NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion type Assertion NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_head.
- NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion description "[After the discovery of JAK and MPL mutations, continual technological advances have led to the identification of increasing numbers of genetic defects in MPN patients, most of them chromosomal aberrations such as deletions and acquired uniparental disomies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_provenance.
- NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion evidence source_evidence_literature NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_provenance.
- NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion SIO_000772 21062246 NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_provenance.
- NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion wasDerivedFrom befree-2016 NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_provenance.
- NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion wasGeneratedBy ECO_0000203 NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_provenance.