Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_provenance.
- NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_assertion description "[Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_provenance.
- NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_assertion evidence source_evidence_literature NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_provenance.
- NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_assertion SIO_000772 23643382 NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_provenance.
- NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_assertion wasDerivedFrom befree-20150227 NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_provenance.
- NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_assertion wasGeneratedBy ECO_0000203 NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP877460.RAQITv-47RVsuQuB1fzGbuWcWniJwoWjVPF2VDEocskx0130_provenance.