Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_provenance.
- NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_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." NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_provenance.
- NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_assertion evidence source_evidence_literature NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_provenance.
- NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_assertion SIO_000772 20593197 NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_provenance.
- NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_assertion wasDerivedFrom befree-20150227 NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_provenance.
- NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_assertion wasGeneratedBy ECO_0000203 NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP987217.RAgVvBpONoNTZHMIY_7QD1ysw__zTKB4YDtUu77PKSJLg130_provenance.