Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_provenance.
- NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_assertion description "[In patient 1 carrying the 14q32 microdeletion, tall stature and renal malformation were unexplained by paternal UPD(14), and there was no altered DLK1 expression or unexpected methylation status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_provenance.
- NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_assertion evidence source_evidence_literature NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_provenance.
- NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_assertion SIO_000772 23552953 NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_provenance.
- NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_assertion wasDerivedFrom befree-20140225 NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_provenance.
- NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_assertion wasGeneratedBy ECO_0000203 NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP417773.RARLCmzVHG-7Rd0K_wVzc74Pmg66EKE3jeVeVXxGTXiD4130_provenance.