Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_assertion wasGeneratedBy ECO_0000203 NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_assertion wasDerivedFrom befree-20140225 NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_assertion SIO_000772 18981294 NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_assertion evidence source_evidence_literature NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_assertion description "[Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.