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- NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_assertion type Assertion NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_head.
- NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_assertion wasGeneratedBy ECO_0000203 NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_provenance.
- NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_assertion wasDerivedFrom befree-2016 NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_provenance.
- NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_assertion SIO_000772 10587520 NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_provenance.
- NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_assertion evidence source_evidence_literature NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_provenance.
- NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_assertion description "[Mutations in human NKX2.5 cause a variety of cardiac anomalies and may account for a clinically significant portion of tetralogy of Fallot and idiopathic AV block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269271.RANwlfFV4ad8FOEZhPnLO6rsk-0juSTo7TBigh4CwFMeQ130_provenance.