Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_provenance.
- NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_assertion wasGeneratedBy ECO_0000203 NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_provenance.
- NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_assertion wasDerivedFrom befree-2016 NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_provenance.
- NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_assertion SIO_000772 20967465 NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_provenance.
- NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_assertion evidence source_evidence_literature NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_provenance.
- NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_assertion description "[In conclusion, we provide evidence that RAB3GAP2 mutations are not specific to Martsolf syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_provenance.