Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_provenance.
- NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_assertion description "[Is loss of heterozygosity at 9q22.3 (PTCH gene) and 19p13.3 (STK11 gene) involved in the pathogenesis of ovarian stromal tumors?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_provenance.
- NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_assertion evidence source_evidence_literature NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_provenance.
- NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_assertion SIO_000772 16084949 NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_provenance.
- NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_assertion wasDerivedFrom befree-2016 NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_provenance.
- NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_assertion wasGeneratedBy ECO_0000203 NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP507765.RAm6qoorkEYNcFlNfgtcpp4FzgwDA03xWx1nwdAtrkhwQ130_provenance.