Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_provenance.
- NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_assertion description "[In search of a genetic linkage between the two immunodeficiencies, we examined the major histocompatibility complex (MHC) class III genes encoding complement components C2, C4A, and C4B and steroid 21-hydroxylase in addition to the HLA serotypes in individuals with either common variable immunodeficiency or IgA deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_provenance.
- NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_assertion evidence source_evidence_literature NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_provenance.
- NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_assertion SIO_000772 2573059 NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_provenance.
- NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_assertion wasDerivedFrom befree-20140225 NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_provenance.
- NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_assertion wasGeneratedBy ECO_0000203 NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP791002.RA1HcSCbwG0AwCgL4L2BcjmBr7Zrbx4qZoYqhz0QzUUE8130_provenance.