Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_provenance.
- NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_assertion description "[The only POR missense polymorphism found in atypical 21OHD patients was A503V.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_provenance.
- NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_assertion evidence source_evidence_literature NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_provenance.
- NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_assertion SIO_000772 18397975 NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_provenance.
- NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_assertion wasDerivedFrom gad-20150221 NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_provenance.
- NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_assertion wasGeneratedBy ECO_0000203 NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP121412.RADYpYpWX7h8kJTkVIyF4v1VEmXGzJqmRN_wHGs4M1EFA130_provenance.