Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_provenance.
- NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_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." NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_provenance.
- NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_assertion evidence source_evidence_literature NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_provenance.
- NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_assertion SIO_000772 15823280 NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_provenance.
- NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_assertion wasDerivedFrom lhgdn-20090331 NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_provenance.
- NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_assertion wasGeneratedBy ECO_0000203 NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP134781.RATvT3Mg7ol8aSMgKoLVrM9_SsaqXsb9d8rPIaNtBgh98130_provenance.