Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_provenance.
- NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_assertion wasGeneratedBy ECO_0000203 NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_provenance.
- NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_assertion wasDerivedFrom gad-20150221 NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_provenance.
- NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_assertion SIO_000772 18599554 NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_provenance.
- NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_assertion evidence source_evidence_literature NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_provenance.
- NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_assertion description "[We confirmed previously found associations between four polymorphisms and CHD, but refuted associations for six other polymorphisms in our large FH population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125718.RAG1AFkhxKjf-2cL0sKSd38FwFd4WTLtm98Sxnku-S1fg130_provenance.