Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_provenance.
- NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_assertion description "[In up to 70% of patients with MDS clonal chromosome abnormalities can be identified which have a high impact on setting the correct diagnosis and estimation of prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_provenance.
- NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_assertion evidence source_evidence_literature NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_provenance.
- NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_assertion SIO_000772 24507811 NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_provenance.
- NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_assertion wasDerivedFrom befree-2016 NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_provenance.
- NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_assertion wasGeneratedBy ECO_0000203 NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1153241.RAxO4p3P8W8XifQMC-grtR5FKXNM-uOO1P3ANiCgQfw_c130_provenance.