Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_provenance.
- NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_assertion description "[Our results suggest the variants of GJC3, GJB4, and GJB3 may be the common genetic risk factor, after variants of GJB2, for the development of nonsyndromic HL in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_provenance.
- NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_assertion evidence source_evidence_literature NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_provenance.
- NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_assertion SIO_000772 20593197 NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_provenance.
- NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_assertion wasDerivedFrom befree-20150227 NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_provenance.
- NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_assertion wasGeneratedBy ECO_0000203 NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426678.RAIm8KefET8miC60K2PzJ_a4m6_qyhuT1BrIZB_nvfG3Y130_provenance.