Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_provenance.
- NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_assertion description "[We examined cell lines from patients with cGKD whose clinical features would be informative and would allow us to determine if IL1RAPL1 deletions can help to explain the MR in patients with deletions extending telomeric from DAX1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_provenance.
- NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_assertion evidence source_evidence_literature NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_provenance.
- NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_assertion SIO_000772 15300857 NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_provenance.
- NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_assertion wasDerivedFrom befree-20140225 NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_provenance.
- NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_assertion wasGeneratedBy ECO_0000203 NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP853080.RA5rxPLKhLk13Q_O5zsZPscS-EBtVsvaqjm65WaP01aIs130_provenance.