Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_assertion> ?p ?o ?g. }
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- NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_assertion type Assertion NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_head.
- NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_assertion description "[Surprisingly, molecular karyotyping to exclude 22q11.2 deletion syndrome in the replication cohort of 17 simplex TA cases revealed a de novo hemizygous deletion that encompasses PRDM1, deficiency of which also results in TA phenotype in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_provenance.
- NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_assertion evidence source_evidence_literature NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_provenance.
- NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_assertion SIO_000772 25713110 NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_provenance.
- NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_assertion wasDerivedFrom befree-2016 NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_provenance.
- NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_assertion wasGeneratedBy ECO_0000203 NP1266167.RAeeY6g7Uh8XGdnLkQPJm2wCGgujxLiBqE5NU9eDLlfE4130_provenance.