Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_assertion> ?p ?o ?g. }
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- NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_assertion type Assertion NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_head.
- NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_assertion wasGeneratedBy ECO_0000203 NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_provenance.
- NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_assertion wasDerivedFrom befree-20140225 NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_provenance.
- NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_assertion SIO_000772 20730472 NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_provenance.
- NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_assertion evidence source_evidence_literature NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_provenance.
- NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_assertion description "[DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656759.RAG5FaTtu68YfJDnt672L0KAkAj_JH6X6UrT8L-P48-Q0130_provenance.