Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance.
- NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_assertion description "[Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance.
- NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_assertion evidence source_evidence_literature NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance.
- NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_assertion SIO_000772 23615299 NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance.
- NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_assertion wasDerivedFrom befree-20140225 NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance.
- NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_assertion wasGeneratedBy ECO_0000203 NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP176039.RAQnmQ0eJQwicq8JjBjI8PqZz-QNWbpH1xcWRhMM8UOGA130_provenance.