Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_provenance.
- NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_assertion description "[Further aims were to compare karyotypic features of t-AML/t-MDS with de novo AML/MDS, in our material as well as in 5098 unselected, cyto- genetically abnormal, published cases, and to analyze associations between type of prior therapy and karyotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_provenance.
- NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_assertion evidence source_evidence_literature NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_provenance.
- NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_assertion SIO_000772 12454741 NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_provenance.
- NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_assertion wasDerivedFrom befree-20150227 NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_provenance.
- NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_assertion wasGeneratedBy ECO_0000203 NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781607.RAxfZL4OYbd9XHCNMsP1LFXmp_UmDkS3gI35ODKZqE-Cw130_provenance.