Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_assertion> ?p ?o ?g. }
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- NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_assertion type Assertion NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_head.
- NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_assertion wasGeneratedBy ECO_0000203 NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_provenance.
- NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_assertion wasDerivedFrom befree-20140225 NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_provenance.
- NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_assertion SIO_000772 11559911 NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_provenance.
- NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_assertion evidence source_evidence_literature NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_provenance.
- NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_assertion description "[Given that molecular investigation of XNP/ATR-X mutations is made onerous by the length of the gene transcript, we carried out a prenatal diagnosis in a fetus at risk for ATR-X syndrome by initially determining the XNP/ATR-X gene haplotype before considering gene sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837522.RAvmmDqr2QOa6tbQU8ZnrYZlgRJ8CB0DVbG9NYgOjOKEs130_provenance.