Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_assertion type Assertion NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_head.
- NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_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." NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance.
- NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_assertion evidence source_evidence_literature NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance.
- NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_assertion SIO_000772 11408949 NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance.
- NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_assertion wasDerivedFrom befree-20140225 NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance.
- NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_assertion wasGeneratedBy ECO_0000203 NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance.