Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_provenance.
- NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_assertion description "[Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_provenance.
- NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_assertion evidence source_evidence_curated NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_provenance.
- NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_assertion SIO_000772 10369266 NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_provenance.
- NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_assertion wasDerivedFrom ctd_human-2016 NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_provenance.
- NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_assertion wasGeneratedBy ECO_0000218 NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP10347.RAdoyOe0S003cUMe_rmmugKXl5T4OBiXlWFA9vTkdOCDo130_provenance.