Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_assertion type Assertion NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_head.
- NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_assertion description "[Several mutations have been identified in ARX gene, which is responsible for a wide spectrum of phenotypes, including syndromic as well as non syndromic forms of mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_provenance.
- NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_assertion evidence source_evidence_literature NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_provenance.
- NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_assertion SIO_000772 16762829 NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_provenance.
- NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_assertion wasDerivedFrom befree-2016 NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_provenance.
- NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_assertion wasGeneratedBy ECO_0000203 NP553800.RAHpi98LKwYYbkAXNfKdQ14gEJPbwmgZpInUxoXSYF-Bg130_provenance.