Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_provenance.
- NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_assertion description "[Mutations detected within the two genes known to be associated with cystinuria, SLC3A1 (related to type I) and SLC7A9 (related to non-type I), cannot, however, in all cases explain the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_provenance.
- NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_assertion evidence source_evidence_literature NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_provenance.
- NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_assertion SIO_000772 14586528 NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_provenance.
- NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_assertion wasDerivedFrom befree-2016 NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_provenance.
- NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_assertion wasGeneratedBy ECO_0000203 NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_provenance.
- befree-2016 importedOn "2016-02-19" NP418764.RAnj4AnbyuuKac06Oss1NBWptckGvKoK3w-wZu_e10Wyg130_provenance.