Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_provenance.
- NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_assertion description "[Common genetic variants in candidate genes and risk of familial lymphoid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_provenance.
- NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_assertion evidence source_evidence_literature NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_provenance.
- NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_assertion SIO_000772 19573080 NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_provenance.
- NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_assertion wasDerivedFrom gad-20130706 NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_provenance.
- NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_assertion wasGeneratedBy ECO_0000203 NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_provenance.
- gad-20130706 importedOn "2013-07-06" NP82138.RAiZwdso2WW_M1AYL4IBeQ1bpdC5lm3hjpDacISoZRwBw130_provenance.