Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP216728.RAtRd2exW0JIDfdgkd2Bo2mgZy4WZBEA6Yl2lHm82uYuk130_provenance.