Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_assertion> ?p ?o ?g. }
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- NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_assertion type Assertion NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_head.
- NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_provenance.
- NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_assertion evidence source_evidence_literature NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_provenance.
- NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_assertion SIO_000772 8744027 NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_provenance.
- NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_assertion wasDerivedFrom befree-20150227 NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_provenance.
- NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_assertion wasGeneratedBy ECO_0000203 NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_provenance.