Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_provenance.
- NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_assertion description "[RTK analysis of all CCS/MM samples showed activation of short-form (sf) recepteur d'origine nantais (RON) RTK and of PDGFRB, MET, and HER3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_provenance.
- NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_assertion evidence source_evidence_literature NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_provenance.
- NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_assertion SIO_000772 22045652 NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_provenance.
- NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_assertion wasDerivedFrom befree-2016 NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_provenance.
- NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_assertion wasGeneratedBy ECO_0000203 NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_provenance.
- befree-2016 importedOn "2016-02-19" NP935461.RAfZWKqtcHEd0fNpleC6QfaOHBqwQekGGQTxZ2OLNDFZM130_provenance.