Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_assertion> ?p ?o ?g. }
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- NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_assertion type Assertion NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_head.
- NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_assertion description "[In our study of sequence variation within the RPGR gene associated with X-linked retinitis pigmentosa, we and others have observed a high rate of new mutation within this gene, as all reported mutations are unique or uncommon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_provenance.
- NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_assertion evidence source_evidence_literature NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_provenance.
- NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_assertion SIO_000772 10980543 NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_provenance.
- NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_assertion wasDerivedFrom befree-2016 NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_provenance.
- NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_assertion wasGeneratedBy ECO_0000203 NP294578.RAr_kxtzd-uJ9l0Z7hd2cUpXKl_nDa_YeoH8QBwwblUPQ130_provenance.