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- source_evidence_literature type ECO_0000212 NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_provenance.
- NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_assertion description "[Mutations in 2 of these genes were shown to cause BFNC (KCNQ3) and hereditary deafness (KCNQ4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_provenance.
- NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_assertion evidence source_evidence_literature NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_provenance.
- NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_assertion SIO_000772 12707061 NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_provenance.
- NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_assertion wasDerivedFrom befree-2016 NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_provenance.
- NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_assertion wasGeneratedBy ECO_0000203 NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP391756.RAbEbezgZRdZryt-rWwPiAfFRHq_XT1cg1Nc_ZXITIpSQ130_provenance.