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- source_evidence_literature type ECO_0000212 NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_provenance.
- NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_assertion description "[In addition, a CDH7 mutation was found in an individual without temporal bone malformation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_provenance.
- NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_assertion evidence source_evidence_literature NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_provenance.
- NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_assertion SIO_000772 18445044 NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_provenance.
- NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_assertion wasDerivedFrom befree-2016 NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_provenance.
- NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_assertion wasGeneratedBy ECO_0000203 NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_provenance.
- befree-2016 importedOn "2016-02-19" NP668455.RAK20iuHpwzRNnc-GxwELWBYQGCwhkpm432oL1M7latu0130_provenance.