Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_provenance.
- NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_assertion description "[We therefore next analyzed compound heterozygote effects in 77 subjects with either hypocretin deficiency or cataplexy and one copy of DRB1*1501-DQA1*0102-DQB1*0602, a sample constructed to maximize etiologic homogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_provenance.
- NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_assertion evidence source_evidence_literature NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_provenance.
- NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_assertion SIO_000772 17207713 NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_provenance.
- NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_assertion wasDerivedFrom befree-20140225 NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_provenance.
- NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_assertion wasGeneratedBy ECO_0000203 NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP791007.RA0DyY3yoMFE7lK1GIMyRKortHNRCI7otdrYL20Q0fF1s130_provenance.