Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_provenance.
- NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_assertion description "[Although there were no pathogenic mutations in DLG4/PSD95 or GABARAP in a cohort study with 142 patients with idiopathic developmental delay with/without epilepsy, further studies would be required for genes included in this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_provenance.
- NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_assertion evidence source_evidence_literature NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_provenance.
- NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_assertion SIO_000772 20111057 NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_provenance.
- NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_assertion wasDerivedFrom befree-2016 NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_provenance.
- NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_assertion wasGeneratedBy ECO_0000203 NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_provenance.
- befree-2016 importedOn "2016-02-19" NP790284.RAmCEeXt31o2UsIJL3XjgvUyahHSOQEhXMsGu1eVVSJDU130_provenance.