Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_provenance.
- NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_assertion description "[This is the first report ever described for patients with CLPD and MDS and/or MPD shown to arise from distinct chromosomal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_provenance.
- NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_assertion evidence source_evidence_literature NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_provenance.
- NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_assertion SIO_000772 11378546 NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_provenance.
- NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_assertion wasDerivedFrom befree-20140225 NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_provenance.
- NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_assertion wasGeneratedBy ECO_0000203 NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651706.RAyddKECEnoPlUPq-lYufw-BR0l-8SPrk34g_aEYvyHew130_provenance.