Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_assertion> ?p ?o ?g. }
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- NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_assertion type Assertion NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_head.
- NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_assertion description "[The purpose of the present study was to determine the utility and limitations of haplotype-based genetic mapping in estimating the location of the NYX gene, which has recently been identified as the causative gene for a rare inherited retinal disorder known as the complete type of X-linked congenital stationary night blindness (CSNB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_provenance.
- NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_assertion evidence source_evidence_literature NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_provenance.
- NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_assertion SIO_000772 11408949 NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_provenance.
- NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_assertion wasDerivedFrom befree-2016 NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_provenance.
- NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_assertion wasGeneratedBy ECO_0000203 NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_provenance.