Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_provenance.
- NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_assertion description "[This study confirmed the very high degree of ABCA4 sequence polymorphism in the general population, which makes the detection of potential disease-associated alleles particularly challenging. While this study does not definitively exclude ABCA4 from contr]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_provenance.
- NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_assertion evidence source_evidence_literature NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_provenance.
- NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_assertion SIO_000772 12824224 NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_provenance.
- NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_assertion wasDerivedFrom gad-20150221 NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_provenance.
- NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_assertion wasGeneratedBy ECO_0000203 NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_provenance.