Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_provenance.
- NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_assertion description "[Mutations in connexin 31 (GJB3) and connexin 30.3 (GJB4), implicated in previous reports of EKV, and connexin 26 (GJB2), implicated in palmoplantar keratoderma, were unlikely given the lack of shared homozygous haplotypes in the regions surrounding these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_provenance.
- NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_assertion evidence source_evidence_literature NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_provenance.
- NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_assertion SIO_000772 15668823 NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_provenance.
- NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_assertion wasDerivedFrom befree-20150227 NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_provenance.
- NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_assertion wasGeneratedBy ECO_0000203 NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968724.RATFWo_VAgp8h6pMsNiDO0OPcUG4_dN2Vn8jknMvhsnv0130_provenance.