Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_provenance.
- NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_assertion description "[We sought to investigate the homozygote haplotype compartment in a recently identified polymorphic purine complex at the upstream region of the human CAV1 gene in multiple sclerosis (MS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_provenance.
- NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_assertion evidence source_evidence_literature NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_provenance.
- NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_assertion SIO_000772 19828204 NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_provenance.
- NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_assertion wasDerivedFrom befree-20140225 NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_provenance.
- NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_assertion wasGeneratedBy ECO_0000203 NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP580282.RAPkPwEWs4_UE5M5a-EtEog2j80h4oXP4Xh0uJiGhdW_w130_provenance.