Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_assertion> ?p ?o ?g. }
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- NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_assertion type Assertion NP847502.RALHwAyHMnnNv984M5ZQTTgIWZtP1hjFGXoEn6U8fcAsQ130_head.
- 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.