Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance.
- NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_assertion description "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance.
- NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_assertion evidence source_evidence_curated NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance.
- NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_assertion SIO_000772 19409524 NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance.
- NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_assertion wasDerivedFrom ctd_human-20150221 NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance.
- NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_assertion wasGeneratedBy ECO_0000218 NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP6809.RACSXaH3_54rYvIKnVVCDiUfTGDdTcR3UAU3GYQ4UzHdI130_provenance.