Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_provenance.
- NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_assertion description "[These deletions are close to the APC and VHL genes that confer susceptibility to familial Adenomatous polyposis (OMIM #17510) and von-Hippel-Lindau syndrome (OMIM #193300), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_provenance.
- NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_assertion evidence source_evidence_literature NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_provenance.
- NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_assertion SIO_000772 17954272 NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_provenance.
- NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_assertion wasDerivedFrom befree-2016 NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_provenance.
- NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_assertion wasGeneratedBy ECO_0000203 NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_provenance.
- befree-2016 importedOn "2016-02-19" NP636759.RAPqdcRPwW0rM6YtoRi_NzrXI6eps72yzKs7rfx_jOwFA130_provenance.