Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_provenance.
- NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_assertion description "[Studies of families with Birt-Hogg-Dub� syndrome (BHD) have recently revealed protein-truncating mutations in the BHD gene, leading to tumorigenesis of the skin and of different cell types of kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_provenance.
- NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_assertion evidence source_evidence_literature NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_provenance.
- NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_assertion SIO_000772 12907635 NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_provenance.
- NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_assertion wasDerivedFrom befree-2016 NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_provenance.
- NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_assertion wasGeneratedBy ECO_0000203 NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_provenance.
- befree-2016 importedOn "2016-02-19" NP404854.RASW7UnanAK5sQ_uylX5pO_e1ff0nRwu1kl25nU_bYNCA130_provenance.