Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_provenance.
- NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_assertion description "[These patients probably carried all, or at least the class II and III regions, of the extended haplotype marked by B8/C4A*Q0/C4B1/BfS/DR3/DR52, which has been associated with several autoimmune diseases and is present in 11% of the healthy caucasoid population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_provenance.
- NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_assertion evidence source_evidence_literature NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_provenance.
- NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_assertion SIO_000772 7923882 NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_provenance.
- NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_assertion wasDerivedFrom befree-20140225 NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_provenance.
- NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_assertion wasGeneratedBy ECO_0000203 NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP719158.RA9W5a2dbE7StvzT85tqpZQbPivYef0a70GzDIl5PIwqE130_provenance.