Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_provenance.
- NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_assertion description "[In addition to celiac disease (CD), type I diabetes, Grave's disease, rheumatoid arthritis and multiple sclerosis have all demonstrated associations to the A/G single nucleotide polymorphism (SNP) in exon 1, position +49 of the CTLA4 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_provenance.
- NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_assertion evidence source_evidence_literature NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_provenance.
- NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_assertion SIO_000772 11098935 NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_provenance.
- NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_assertion wasDerivedFrom befree-2016 NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_provenance.
- NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_assertion wasGeneratedBy ECO_0000203 NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_provenance.
- befree-2016 importedOn "2016-02-19" NP301776.RA1T5u1kB7Oy4AO3IgdXvbfyK9rXgPoW1keMLX4M2Sj54130_provenance.