Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_provenance.
- NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_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." NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_provenance.
- NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_assertion evidence source_evidence_literature NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_provenance.
- NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_assertion SIO_000772 20593197 NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_provenance.
- NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_assertion wasDerivedFrom befree-20140225 NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_provenance.
- NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_assertion wasGeneratedBy ECO_0000203 NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP278163.RAUiElSYBAX3lgFr1_CSSdsoEwbjrY1tmS_ctYq_LXENY130_provenance.