Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_provenance.
- NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_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." NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_provenance.
- NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_assertion evidence source_evidence_literature NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_provenance.
- NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_assertion SIO_000772 21712540 NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_provenance.
- NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_assertion wasDerivedFrom befree-20150227 NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_provenance.
- NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_assertion wasGeneratedBy ECO_0000203 NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978557.RAb95gfJxhHCVoEQeEUXcXLinHlo7aGGkgw7go6WbBJUM130_provenance.