Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_provenance.
- NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_assertion description "[75 different LDL receptor mutations in 645 children with heterozygous familial hypercholesterolemia; in these children, null alleles were clearly associated with more elevated LDL cholesterol levels compared to receptor-defective mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_provenance.
- NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_assertion evidence source_evidence_literature NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_provenance.
- NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_assertion SIO_000772 15823280 NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_provenance.
- NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_assertion wasDerivedFrom lhgdn-20090331 NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_provenance.
- NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_assertion wasGeneratedBy ECO_0000203 NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP210241.RA_dEAtod195X-pqIYczWxfZBWZvatfLdEfgKLalbXIOE130_provenance.