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- source_evidence_literature type ECO_0000212 NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_provenance.
- NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_assertion description "[We identified three girls with classical CFNS and mild developmental delay harboring de novo deletions of the EFNB1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_provenance.
- NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_assertion evidence source_evidence_literature NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_provenance.
- NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_assertion SIO_000772 17941886 NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_provenance.
- NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_assertion wasDerivedFrom befree-2016 NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_provenance.
- NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_assertion wasGeneratedBy ECO_0000203 NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_provenance.
- befree-2016 importedOn "2016-02-19" NP635690.RAsZeCAGLZ88dmp6rH2sm8W-CwyeRDqORWbS5OJo9K21w130_provenance.