Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_assertion> ?p ?o ?g. }
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- NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_assertion type Assertion NP13502.RAe-WvCA6a0Jc9OI0NSOCZHtPqwJ9qLN3P_dPBBtQ9txg130_head.
- 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.