Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_assertion> ?p ?o ?g. }
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- NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_assertion type Assertion NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_head.
- NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_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." NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_provenance.
- NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_assertion evidence source_evidence_literature NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_provenance.
- NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_assertion SIO_000772 9824441 NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_provenance.
- NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_assertion wasDerivedFrom befree-20150227 NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_provenance.
- NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_assertion wasGeneratedBy ECO_0000203 NP247309.RAcBMVrYoQu3hA388I7Sca_l4hW5LbjZkXUpnqaceZrqM130_provenance.