Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_assertion> ?p ?o ?g. }
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- NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_assertion type Assertion NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_head.
- NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_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." NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_provenance.
- NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_assertion evidence source_evidence_literature NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_provenance.
- NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_assertion SIO_000772 18463683 NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_provenance.
- NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_assertion wasDerivedFrom gad-20130706 NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_provenance.
- NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_assertion wasGeneratedBy ECO_0000203 NP78982.RAtf0QhYEphtqTB3EuIK0vSqz4pEDD_Lvt8YuUEy-a27c130_provenance.