Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance.