Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion description "[ZFHX1B mutations cause a complex developmental phenotype characterized by severe mental retardation (MR) and multiple congenital defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion evidence source_evidence_literature NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion SIO_000772 15006694 NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion wasDerivedFrom befree-20150227 NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_assertion wasGeneratedBy ECO_0000203 NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831130.RAgxGTL58GneB3y3byn6iVsu0Qt3XG0FAe0t9-S4WlBZU130_provenance.