Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_provenance.
- befree-2016 importedOn "2016-02-19" NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_provenance.
- NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_assertion wasGeneratedBy ECO_0000203 NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_provenance.
- NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_assertion wasDerivedFrom befree-2016 NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_provenance.
- NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_assertion SIO_000772 20687945 NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_provenance.
- NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_assertion evidence source_evidence_literature NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_provenance.
- NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_assertion description "[Here, we describe a screening method, HRM, for the detection of both heterozygous and homozygous mutations in the gene encoding MUTYH in selected samples of patients with phenotype of MAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831034.RADNIEojylRUCvNsWyWKKD4zRyxJeF_wAQwQSNGrQUwfU130_provenance.