Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_provenance.
- NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_assertion wasGeneratedBy ECO_0000203 NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_provenance.
- NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_assertion wasDerivedFrom befree-20140225 NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_provenance.
- NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_assertion SIO_000772 17855451 NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_provenance.
- NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_assertion evidence source_evidence_literature NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_provenance.
- NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_assertion description "[However, the first mutation reported to cause PCWH was a disruption of the native stop codon that by conceptual translation extends the protein into the 3' untranslated region (3'-UTR) for an additional 82 residues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP533063.RAbxAKyoccs89mZwZ3yO6RZW-Sbc9jEaQ4zksPIii4Bdc130_provenance.