Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion> ?p ?o ?g. }
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- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion type Assertion NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_head.
- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion description "[X-linked isolated lissencephaly sequence (ILS) and subcortical band heterotopia are allelic human disorders associated with mutations of the DCX gene in both familial and sporadic forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion evidence source_evidence_literature NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion SIO_000772 11468322 NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion wasDerivedFrom befree-2016 NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.
- NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_assertion wasGeneratedBy ECO_0000203 NP324900.RAAo-NRV77U15hh41v7_a-CGsBB0wyzGMDGaBS0xvUaYQ130_provenance.