Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_assertion> ?p ?o ?g. }
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- NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_assertion type Assertion NP80342.RA6LgECrBQcSXRAc5qK_DZVHE4K7IN_LFuqN73l8SeTZI130_head.
- 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.