Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP807082.RAo3ZDKhmzq2-xqrdtRLW_9ySYmM5LbSvm_lXRLkovrgw130_provenance.