Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_provenance.
- NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_assertion description "[To begin understanding the molecular basis for ARX mutations, we tested the DNA binding sequence preference and transcriptional repression activity for Arx, deletion mutants and mutants associated with various neurologic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_provenance.
- NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_assertion evidence source_evidence_literature NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_provenance.
- NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_assertion SIO_000772 22252899 NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_provenance.
- NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_assertion wasDerivedFrom befree-20140225 NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_provenance.
- NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_assertion wasGeneratedBy ECO_0000203 NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP756060.RAMfv21pwkoGIY6oBVI5mnkSUWPZMKRGD0m4YVs8-gRV4130_provenance.