Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_assertion> ?p ?o ?g. }
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- NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_assertion type Assertion NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_head.
- NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_assertion description "[The combined results indicate, for the first time, that ACTC1 mutations or reduced ACTC1 levels may lead to ASD without signs of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_provenance.
- NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_assertion evidence source_evidence_literature NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_provenance.
- NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_assertion SIO_000772 17947298 NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_provenance.
- NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_assertion wasDerivedFrom befree-20140225 NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_provenance.
- NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_assertion wasGeneratedBy ECO_0000203 NP771758.RAcSf1yrOhZA39KDomqpGyV_IeoFhnqNX5TseanHTgnF8130_provenance.