Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion wasGeneratedBy ECO_0000203 NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion wasDerivedFrom befree-20140225 NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion SIO_000772 11851376 NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion evidence source_evidence_literature NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion description "[DNA samples of 98 unrelated Belgian patients with a family history of autosomal dominant hypercholesterolaemia were screened for mutations in the LDLR gene, after exclusion of known mutations causing familial defective apolipoprotein B-100 (FDB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.