Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_provenance.
- NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_assertion description "[Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the `Mowat-Wilson` syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_provenance.
- NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_assertion evidence source_evidence_curated NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_provenance.
- NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_assertion SIO_000772 15006694 NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_provenance.
- NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_assertion wasDerivedFrom ctd_human-20130708 NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_provenance.
- NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_assertion wasGeneratedBy ECO_0000218 NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP33991.RAD32I34gfOHKJCJbZkCRv-d2NOGDNRKC45vrBRM-numQ130_provenance.