Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_provenance.
- NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_assertion description "[Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_provenance.
- NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_assertion evidence source_evidence_curated NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_provenance.
- NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_assertion SIO_000772 14608643 NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_provenance.
- NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_assertion wasDerivedFrom ctd_human-2016 NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_provenance.
- NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_assertion wasGeneratedBy ECO_0000218 NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_provenance.