Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_provenance.
- NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_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." NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_provenance.
- NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_assertion evidence source_evidence_literature NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_provenance.
- NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_assertion SIO_000772 7923882 NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_provenance.
- NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_assertion wasDerivedFrom befree-2016 NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_provenance.
- NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_assertion wasGeneratedBy ECO_0000203 NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327145.RAbWqwpfvQr9VSluGjlKJioQkAY8M6WyfDb3SGpzmL-lE130_provenance.