Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance.
- NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_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." NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance.
- NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_assertion evidence source_evidence_curated NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance.
- NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_assertion SIO_000772 19409524 NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance.
- NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_assertion wasDerivedFrom ctd_human-20130708 NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance.
- NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_assertion wasGeneratedBy ECO_0000218 NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP8551.RAH11z6sdPUzibUgJNmTZBCyawSY2CUwEJgEdFZepa750130_provenance.