Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_provenance.
- NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_assertion description "[We found twelve individuals with the JAK2 V617F mutation; five of them had been clinically classified as PV, five as ET, and one as MF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_provenance.
- NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_assertion evidence source_evidence_literature NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_provenance.
- NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_assertion SIO_000772 25637689 NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_provenance.
- NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_assertion wasDerivedFrom befree-2016 NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_provenance.
- NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_assertion wasGeneratedBy ECO_0000203 NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1259775.RAzau1T4QkxrxekBn7dQd9PekH9fEOYECVMTcyGjkrW_Y130_provenance.