Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP697351.RARpu4uSj9ijn7lnSR1zMT-4TnLrao_3UpwFMWRFUIs2o130_provenance.