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- source_evidence_literature type ECO_0000212 NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_provenance.
- NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_assertion description "[On the basis of these analyses, we conclude that the phenotypic spectrum of ZIC3 mutations should be expanded to include affected females and CHD not typical for heterotaxy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_provenance.
- NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_assertion evidence source_evidence_literature NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_provenance.
- NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_assertion SIO_000772 14681828 NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_provenance.
- NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_assertion wasDerivedFrom befree-2016 NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_provenance.
- NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_assertion wasGeneratedBy ECO_0000203 NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_provenance.
- befree-2016 importedOn "2016-02-19" NP425148.RAVZzkUUjvIwzIl-0RObVdTL0THZw75gmJxnUyseGpQDg130_provenance.