Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_provenance.
- NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_assertion description "[Whole-exome sequencing of a single Italian proband affected by non-syndromic HL identified a novel missense variant within the PRPS1 gene (NM_002764.3:c.337G>T (p.A113S)) segregating with post-lingual, bilateral, progressive deafness in the proband's family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_provenance.
- NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_assertion evidence source_evidence_literature NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_provenance.
- NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_assertion SIO_000772 25182139 NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_provenance.
- NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_assertion wasDerivedFrom befree-2016 NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_provenance.
- NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_assertion wasGeneratedBy ECO_0000203 NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216221.RAyyUxqzyXSnfaWTZEDt4PsIhylk2TC0GG3pgCIakw7_8130_provenance.