Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_provenance.
- NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_assertion description "[Familial hypercholesterolaemia (FH) is a common autosomal codominant hereditary disease caused by defects in the LDL receptor (LDLR) gene, and one of the most common characteristics of affected subjects is premature coronary heart disease (CHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_provenance.
- NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_assertion evidence source_evidence_literature NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_provenance.
- NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_assertion SIO_000772 12624133 NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_provenance.
- NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_assertion wasDerivedFrom befree-20140225 NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_provenance.
- NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_assertion wasGeneratedBy ECO_0000203 NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP542148.RAWdXmcmVqvj021wLt5z22cbofPqCwrN0rXe_p6KGAnBA130_provenance.