Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_provenance.
- NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_assertion description "[We identified homozygous deletion of p16 and p15 genes in five (19%) of 27 acute lymphoblastic leukemias (ALLs) and in two (11%) of 19 acute myeloid leukemias (AMLs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_provenance.
- NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_assertion evidence source_evidence_literature NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_provenance.
- NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_assertion SIO_000772 9447829 NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_provenance.
- NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_assertion wasDerivedFrom befree-2016 NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_provenance.
- NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_assertion wasGeneratedBy ECO_0000203 NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1387825.RA7JXH1lLiKlAAss7fcSLBaZMzRDM1tdUhuIf1osskyp4130_provenance.