Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_provenance.
- NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_assertion description "[A novel ribosomal S6-kinase (RSK4; RPS6KA6) is commonly deleted in patients with complex X-linked mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_provenance.
- NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_assertion evidence source_evidence_literature NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_provenance.
- NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_assertion SIO_000772 10644430 NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_provenance.
- NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_assertion wasDerivedFrom befree-2016 NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_provenance.
- NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_assertion wasGeneratedBy ECO_0000203 NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_provenance.
- befree-2016 importedOn "2016-02-19" NP273071.RA_vNQajapeBaDNRIJDpuvofjaYfcmWetiPYzNbYlfsKw130_provenance.