Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_provenance.
- NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_assertion description "[The PITX3 gene, which codes for a homeobox bicoidlike transcription factor is responsible for dominant cataract and anterior segment mesenchymal dysgenesis in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_provenance.
- NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_assertion evidence source_evidence_curated NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_provenance.
- NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_assertion SIO_000772 16565358 NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_provenance.
- NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_assertion wasDerivedFrom ctd_human-20130708 NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_provenance.
- NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_assertion wasGeneratedBy ECO_0000218 NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP26013.RAejWq4QR71zqEdj2yA4LYl2FsdSGVhbQxR-NZC6f_Dr0130_provenance.