Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion description "[The common aberration found in these two t-MDS cases was the fragility of chromosome 5 and monosomy of chromosome 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion evidence source_evidence_literature NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion SIO_000772 12505257 NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion wasDerivedFrom befree-20150227 NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_assertion wasGeneratedBy ECO_0000203 NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978519.RAiMTRbx3bt5-WYocQeO9uS4wQt4n-g1ruDpFq6oo0-Jc130_provenance.