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- source_evidence_literature type ECO_0000212 NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_provenance.
- NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_assertion description "[With regard to genotype-phenotype correlation, patients with a mutation in the BBS6, BBS10, or BBS12 gene (10 of 33 patients) had more severe renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_provenance.
- NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_assertion evidence source_evidence_literature NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_provenance.
- NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_assertion SIO_000772 20876674 NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_provenance.
- NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_assertion wasDerivedFrom befree-2016 NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_provenance.
- NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_assertion wasGeneratedBy ECO_0000203 NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_provenance.
- befree-2016 importedOn "2016-02-19" NP842208.RA9pynmrONFQgozrsXQmrrSFRdG3BMx1XnalJCBr9__vU130_provenance.