Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance.
- NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_assertion description "[Despite the relevance of both pathways in the pathogenesis of the disease, and the fact that this is indeed the first study that considers these pathways as a candidate-gene selection approach, our study does not present any evidence of the presence of low-penetrance variants for the selected markers in any of the considered genes in our cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance.
- NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_assertion evidence source_evidence_literature NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance.
- NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_assertion SIO_000772 20844743 NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance.
- NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_assertion wasDerivedFrom gad-20130706 NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance.
- NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_assertion wasGeneratedBy ECO_0000203 NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance.
- gad-20130706 importedOn "2013-07-06" NP48539.RAq5bsyXsF2i1oK_SXq7one268jLQr9mDuxHHEk6dHpnw130_provenance.