Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_assertion> ?p ?o ?g. }
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- NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_assertion type Assertion NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_head.
- NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_assertion description "[Currently, SHOX mutations occur with an estimated incidence of roughly 1 in 1000 newborns, making mutations of this gene one of the most common genetic defects associated with growth failure and skeletal deformities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_provenance.
- NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_assertion evidence source_evidence_literature NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_provenance.
- NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_assertion SIO_000772 19724992 NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_provenance.
- NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_assertion wasDerivedFrom befree-20140225 NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_provenance.
- NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_assertion wasGeneratedBy ECO_0000203 NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_provenance.