Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_provenance.
- NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_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." NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_provenance.
- NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_assertion evidence source_evidence_literature NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_provenance.
- NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_assertion SIO_000772 23643382 NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_provenance.
- NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_assertion wasDerivedFrom befree-2016 NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_provenance.
- NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_assertion wasGeneratedBy ECO_0000203 NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1074865.RAAGk2UaZACHE-rrg1tT7D6punisxzGayvGiQXhAN7SSs130_provenance.