Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_provenance.
- NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_assertion wasGeneratedBy ECO_0000218 NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_provenance.
- NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_assertion wasDerivedFrom ctd_human-20130708 NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_provenance.
- NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_assertion SIO_000772 20493458 NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_provenance.
- NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_assertion evidence source_evidence_curated NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_provenance.
- NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_assertion description "[Because not all of our patients harbored mutations in IFT122, CED seems to be genetically heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP19232.RAC35WH9gFk6B3QlvXRhIqd5oaQgR4zH1itCcuCmca0n4130_provenance.