Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_provenance.
- NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_assertion wasGeneratedBy ECO_0000203 NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_provenance.
- NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_assertion wasDerivedFrom gad-20150221 NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_provenance.
- NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_assertion SIO_000772 19319977 NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_provenance.
- NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_assertion evidence source_evidence_literature NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_provenance.
- NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_assertion description "[The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP114799.RAI_JylA_G1ERHLZ_l8IlCtPFrRhXIVRs4YnbJ6kTEOFQ130_provenance.