Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_provenance.
- NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_assertion description "[Brain magnetic resonance imaging (MRI) of all patients showed no brain malformations in contrast to the patients with a premature termination mutation in other exons of ARX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_provenance.
- NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_assertion evidence source_evidence_literature NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_provenance.
- NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_assertion SIO_000772 20384723 NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_provenance.
- NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_assertion wasDerivedFrom befree-2016 NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_provenance.
- NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_assertion wasGeneratedBy ECO_0000203 NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_provenance.
- befree-2016 importedOn "2016-02-19" NP805573.RAiO3yoXM_8IW1IxFoEZjUTpNsN1OwmvflzGsVRMn8PEI130_provenance.