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- source_evidence_literature type ECO_0000212 NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_provenance.
- NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_assertion description "[Mowat-Wilson syndrome (MWS) is an autosomal dominant developmental disorder with mental retardation and variable multiple congenital abnormalities due to mutations of the ZEB2 (ZFHX1B) gene at 2q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_provenance.
- NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_assertion evidence source_evidence_literature NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_provenance.
- NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_assertion SIO_000772 18445050 NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_provenance.
- NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_assertion wasDerivedFrom befree-20150227 NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_provenance.
- NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_assertion wasGeneratedBy ECO_0000203 NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831016.RApR3467nrVhRpwicLnIii_StKEHGCyic1WDohGKVVPoE130_provenance.