Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_provenance.
- NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_assertion description "[SAP mutations have been found in a few patients diagnosed previously as CVID, suggesting that XLP may mimic CVID, but no large-scale analysis of CVID patients has been undertaken.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_provenance.
- NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_assertion evidence source_evidence_literature NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_provenance.
- NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_assertion SIO_000772 15320910 NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_provenance.
- NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_assertion wasDerivedFrom befree-20140225 NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_provenance.
- NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_assertion wasGeneratedBy ECO_0000203 NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP429522.RAQdqXiRe5uG400SWnZh7hux52C3_tbuVRfmHlzYbychk130_provenance.