Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_provenance.
- NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_assertion description "[We found a high incidence of ASXL1 mutation in MF patients (20%) and a low incidence in PV (7%) and ET (4%) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_provenance.
- NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_assertion evidence source_evidence_literature NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_provenance.
- NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_assertion SIO_000772 22489043 NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_provenance.
- NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_assertion wasDerivedFrom befree-20140225 NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_provenance.
- NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_assertion wasGeneratedBy ECO_0000203 NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP410468.RAIxGLVjlniTGea5xZrpuY9ScxLpsTfH6QrggMvSNHVwg130_provenance.