Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_assertion> ?p ?o ?g. }
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- NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_assertion type Assertion NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_head.
- NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_assertion description "[Aristaless-related homeobox (ARX) gene mutations cause a diverse spectrum of disorders of the human brain, including lissencephaly, various forms of epilepsy and non-syndromic mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_provenance.
- NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_assertion evidence source_evidence_literature NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_provenance.
- NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_assertion SIO_000772 19738637 NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_provenance.
- NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_assertion wasDerivedFrom befree-2016 NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_provenance.
- NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_assertion wasGeneratedBy ECO_0000203 NP762182.RA_dUSZaiZYfA1f1WfeaJOtbGkVwEctdBfVULUtDQ9QyE130_provenance.