Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_assertion type Assertion NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_head.
- NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_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." NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_provenance.
- NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_assertion evidence source_evidence_literature NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_provenance.
- NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_assertion SIO_000772 18463683 NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_provenance.
- NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_assertion wasDerivedFrom befree-20150227 NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_provenance.
- NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_assertion wasGeneratedBy ECO_0000203 NP464579.RAd90RjX8h_z05R7kZmL7iP7LL6qP3bHUQ-DS5Ekn--jc130_provenance.