Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_provenance.
- NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_assertion description "[Since the associated HLA-DRB1*1501-DQB1*0602 haplotype is common in the general population (15-25%), it has been suggested that it is almost necessary but not sufficient for developing narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_provenance.
- NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_assertion evidence source_evidence_curated NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_provenance.
- NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_assertion SIO_000772 20711174 NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_provenance.
- NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_assertion wasDerivedFrom ctd_human-20130708 NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_provenance.
- NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_assertion wasGeneratedBy ECO_0000218 NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP18042.RAHW1J_aFF3-dRX080MRSd0bfrcsrxE9LUaUc_nVFtouU130_provenance.