Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_provenance.
- NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_assertion description "[RTL is shorter in affected members with FNMTC but is not associated with altered copy number or expression in hTERT, TRF1, TRF2, RAP1, TIN2, TPP1, and POT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_provenance.
- NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_assertion evidence source_evidence_literature NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_provenance.
- NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_assertion SIO_000772 23009101 NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_provenance.
- NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_assertion wasDerivedFrom befree-20140225 NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_provenance.
- NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_assertion wasGeneratedBy ECO_0000203 NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP488855.RAGhUGzqhqfl6n7rJrQinW8BL2CN0TI4kztbafFm7SkyY130_provenance.