Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_assertion> ?p ?o ?g. }
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- NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_assertion type Assertion NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_head.
- NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_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." NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_provenance.
- NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_assertion evidence source_evidence_literature NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_provenance.
- NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_assertion SIO_000772 17207713 NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_provenance.
- NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_assertion wasDerivedFrom befree-2016 NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_provenance.
- NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_assertion wasGeneratedBy ECO_0000203 NP587553.RATiRh00eC79QHBRaaeZ4W-BZGplSAHd2Zs7ZKXEW6vYs130_provenance.