Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_provenance.
- NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_assertion description "[Although in vitro experiments using Xenopus oocytes have suggested that p.[V27I;E114G] disturbs the gap junction function of Cx26, the equal distribution of this complex allele in both deaf probands and hearing controls makes it a less likely cause of profound congenital deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_provenance.
- NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_assertion evidence source_evidence_literature NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_provenance.
- NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_assertion SIO_000772 20201936 NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_provenance.
- NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_assertion wasDerivedFrom befree-20150227 NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_provenance.
- NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_assertion wasGeneratedBy ECO_0000203 NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426468.RAyg_JgcHiea8iGuFsWGfebJ47JdbN30FN_QK0TvD4VlQ130_provenance.