Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_assertion> ?p ?o ?g. }
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- NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_assertion type Assertion NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_head.
- NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_assertion description "[ZFHX1B mutations cause a complex developmental phenotype characterized by severe mental retardation (MR) and multiple congenital defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_provenance.
- NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_assertion evidence source_evidence_literature NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_provenance.
- NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_assertion SIO_000772 15006694 NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_provenance.
- NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_assertion wasDerivedFrom befree-20140225 NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_provenance.
- NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_assertion wasGeneratedBy ECO_0000203 NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_provenance.