Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_provenance.
- NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_assertion description "[The DQB1*0602 association was highest in cases with hypocretin deficiency (100% vs 13% in controls), most of which had narcolepsy-cataplexy (81%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_provenance.
- NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_assertion evidence source_evidence_literature NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_provenance.
- NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_assertion SIO_000772 17207713 NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_provenance.
- NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_assertion wasDerivedFrom befree-20150227 NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_provenance.
- NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_assertion wasGeneratedBy ECO_0000203 NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP445196.RA575r7b6NoeeIIwXTcggwwUpKUcLohcunal2IeNRjLMM130_provenance.