Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_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." NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_assertion evidence source_evidence_literature NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_assertion SIO_000772 18445050 NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_assertion wasDerivedFrom befree-20140225 NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_assertion wasGeneratedBy ECO_0000203 NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP447616.RAqiFNF6kSQPbU7abHtunmDBxvSZtzF48QMdcU_AYSPuk130_provenance.