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- source_evidence_literature type ECO_0000212 NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_provenance.
- NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_assertion wasGeneratedBy ECO_0000203 NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_provenance.
- NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_assertion wasDerivedFrom lhgdn-20090331 NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_provenance.
- NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_assertion SIO_000772 16550584 NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_provenance.
- NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_assertion evidence source_evidence_literature NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_provenance.
- NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_provenance.