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- source_evidence_literature type ECO_0000212 NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_provenance.
- NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_assertion wasGeneratedBy ECO_0000203 NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_provenance.
- NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_assertion wasDerivedFrom befree-2016 NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_provenance.
- NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_assertion SIO_000772 11549681 NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_provenance.
- NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_assertion evidence source_evidence_literature NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_provenance.
- NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_assertion description "[Autosomal recessive segregation of a truncating mutation of anti-Müllerian type II receptor in a family affected by the persistent Müllerian duct syndrome contrasts with its dominant negative activity in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_provenance.