Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_provenance.
- NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_assertion description "[NSCLC Driven by DDR2 Mutation Is Sensitive to Dasatinib and JQ1 Combination Therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_provenance.
- NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_assertion evidence source_evidence_curated NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_provenance.
- NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_assertion SIO_000772 26206333 NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_provenance.
- NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_assertion wasDerivedFrom ctd_human-2016 NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_provenance.
- NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_assertion wasGeneratedBy ECO_0000218 NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP35622.RAA2PPHZhUkc_Kjux7jvm1CzdcoBGVWyrd9a4STzPA17c130_provenance.