Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_assertion> ?p ?o ?g. }
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- NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_assertion type Assertion NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_head.
- NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_assertion description "[Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_provenance.
- NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_assertion evidence source_evidence_literature NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_provenance.
- NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_assertion SIO_000772 23161826 NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_provenance.
- NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_assertion wasDerivedFrom befree-20150227 NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_provenance.
- NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_assertion wasGeneratedBy ECO_0000203 NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_provenance.