Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_provenance.
- NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_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." NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_provenance.
- NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_assertion evidence source_evidence_curated NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_provenance.
- NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_assertion SIO_000772 15006694 NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_provenance.
- NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_assertion wasDerivedFrom ctd_human-2016 NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_provenance.
- NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_assertion wasGeneratedBy ECO_0000218 NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP13847.RAup6opayaFh0qstwtaN28q-iAqh78EOsL1hm8Y-7bxoo130_provenance.