Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_provenance.
- NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_assertion description "[To assess the prevalence of different forms of OCA and different gene mutations among non-Hispanic Caucasian patients, we performed DNA sequence analysis of the four genes associated with classical OCA (TYR, OCA2, TYRP1, SLC45A2), the two principal genes associated with syndromic OCA (HPS1, HPS4), and a candidate OCA gene (SILV), in 121 unrelated, unselected non-Hispanic/Latino Caucasian patients carrying the clinical diagnosis of OCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_provenance.
- NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_assertion evidence source_evidence_literature NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_provenance.
- NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_assertion SIO_000772 18463683 NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_provenance.
- NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_assertion wasDerivedFrom gad-20150221 NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_provenance.
- NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_assertion wasGeneratedBy ECO_0000203 NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP122850.RAd2TyWjubd94djLC1LuUPg756xQ7V16gucieqH7SNbUI130_provenance.