Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_assertion> ?p ?o ?g. }
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- NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_assertion type Assertion NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_head.
- NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_assertion description "[We therefore screened the WAS gene in 14 young SCN males with wild-type ELA2 and identified 2 with novel mutations, one who presented with myelodysplasia (Ile294Thr) and the other with classic SCN (Ser270Pro).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_provenance.
- NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_assertion evidence source_evidence_literature NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_provenance.
- NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_assertion SIO_000772 16804117 NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_provenance.
- NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_assertion wasDerivedFrom befree-20150227 NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_provenance.
- NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_assertion wasGeneratedBy ECO_0000203 NP372748.RAwQKHDYN8lVh3uq_7vnzt8hrBGi3JZB0GEt9ZUZi7OKs130_provenance.