Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_provenance.
- NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_assertion description "[Somatic missense mutations affecting the RNase IIIb domain of DICER1 are common in nonepithelial ovarian tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_provenance.
- NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_assertion evidence source_evidence_literature NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_provenance.
- NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_assertion SIO_000772 22187960 NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_provenance.
- NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_assertion wasDerivedFrom befree-2016 NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_provenance.
- NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_assertion wasGeneratedBy ECO_0000203 NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_provenance.
- befree-2016 importedOn "2016-02-19" NP948357.RAbVLv7mjFbcb49k4kWmZj2o-HmiRREPoxErn1Na2Sut8130_provenance.