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- source_evidence_literature type ECO_0000212 NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_provenance.
- NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_assertion description "[Therefore, a comprehensive genome-wide analysis of patients with AML or MDS with complex karyotypes has led to a better characterization of chromosomal aberrations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_provenance.
- NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_assertion evidence source_evidence_literature NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_provenance.
- NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_assertion SIO_000772 16142824 NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_provenance.
- NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_assertion wasDerivedFrom befree-2016 NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_provenance.
- NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_assertion wasGeneratedBy ECO_0000203 NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_provenance.
- befree-2016 importedOn "2016-02-19" NP512170.RA79mybz_lGUqmFZ0prm0pAdPt-CzS1hs21urUdUDNSAE130_provenance.