Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_assertion> ?p ?o ?g. }
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- NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_assertion type Assertion NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_head.
- NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_assertion wasGeneratedBy ECO_0000203 NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_provenance.
- NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_assertion wasDerivedFrom befree-2016 NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_provenance.
- NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_assertion SIO_000772 11574150 NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_provenance.
- NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_assertion evidence source_evidence_literature NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_provenance.
- NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_assertion description "[Although the UFD1L gene has been mapped in the region commonly deleted in patients with DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), correlation between its haploinsufficiency and the phenotype has not yet been established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331259.RABilCDV_d1LI0Uh-At-VmKFpXYjIAE1M6CsstUdlQAb8130_provenance.