Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_provenance.
- NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_assertion description "[Functional LDLR mutations occurred in 31 (60%) subjects, who received a diagnosis of familial hypercholesterolemia (FH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_provenance.
- NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_assertion evidence source_evidence_literature NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_provenance.
- NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_assertion SIO_000772 17566095 NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_provenance.
- NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_assertion wasDerivedFrom lhgdn-20090331 NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_provenance.
- NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_assertion wasGeneratedBy ECO_0000203 NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP226207.RAHpkk1U1icQS66LsrDG2tGSoJRMmhAQ_bLIjS3s7nzP0130_provenance.