Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_assertion> ?p ?o ?g. }
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- NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_assertion type Assertion NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_head.
- NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_assertion description "[Carrier testing was performed in 35 women belonging to 16 unrelated Spanish families with at least one subject affected by the Lesch-Nyhan syndrome (11 families, 14 patients) or the Kelley-Seegmiller syndrome (five families, six patients) by means of HPRT and adenine phosphoribosyltransferase activities in hair follicles and/or molecular studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_provenance.
- NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_assertion evidence source_evidence_literature NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_provenance.
- NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_assertion SIO_000772 9824441 NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_provenance.
- NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_assertion wasDerivedFrom befree-2016 NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_provenance.
- NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_assertion wasGeneratedBy ECO_0000203 NP1409338.RAIHMUt-uAW8yl9Hmksjih0qzcmWW04vBO-0JZR98L2us130_provenance.