Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_provenance.
- NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_assertion description "[We propose MYH10 detection as a new and simple tool to identify inherited platelet disorders and myeloid neoplasms with abnormalities in RUNX1 and its associated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_provenance.
- NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_assertion evidence source_evidence_literature NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_provenance.
- NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_assertion SIO_000772 22677128 NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_provenance.
- NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_assertion wasDerivedFrom befree-20140225 NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_provenance.
- NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_assertion wasGeneratedBy ECO_0000203 NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP206345.RAoHaulK_x3X9-R3dkw3-8nmN8jTYABerLcTa10BEj8pA130_provenance.