Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_provenance.
- NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_assertion description "[Exon 12 of ASXL1 was amplified from neutrophil genomic DNA and bidirectionally sequenced in 77 patients with myelofibrosis (including patients with primary and post-essential thrombocytosis or post-polycythemia myelofibrosis), 42 patients with polycythemia vera, 41 with essential thrombocytosis and 6 with post-myelofibrosis acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_provenance.
- NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_assertion evidence source_evidence_literature NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_provenance.
- NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_assertion SIO_000772 21712540 NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_provenance.
- NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_assertion wasDerivedFrom befree-20140225 NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_provenance.
- NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_assertion wasGeneratedBy ECO_0000203 NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP236228.RAggCLXezmGXT7sbGhz0fCOf3Fb2n3j-UhDBsaQYL3UKU130_provenance.