Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion description "[To extend these results we searched for mutations of ASXL1 in a series of chronic myelomonocytic leukaemias, a disease classified as MDS/Myeloproliferative disorder, and found mutations in 17 out of 39 patients (43%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion evidence source_evidence_literature NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion SIO_000772 19388938 NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion wasDerivedFrom befree-20150227 NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion wasGeneratedBy ECO_0000203 NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.