Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_provenance.
- NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_assertion description "[The spectrum of DNA sequence alterations in the hypoxanthine-guanine phosphoribosyltransferase (hprt) gene of HPRTase-deficient T-lymphocytes isolated from the blood of healthy male donors was determined and compared with the spectrum found in patients suffering from genetic diseases (Lesch-Nyhan syndrome or gouty arthritis) associated with a mutation in the same gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_provenance.
- NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_assertion evidence source_evidence_literature NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_provenance.
- NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_assertion SIO_000772 2385250 NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_provenance.
- NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_assertion wasDerivedFrom befree-2016 NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_provenance.
- NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_assertion wasGeneratedBy ECO_0000203 NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1093737.RAtbh2Q7aBR-dguaD3T6fT7f0QuKnEZBeOgKUpHnYnLLE130_provenance.