Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_assertion> ?p ?o ?g. }
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- NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_assertion type Assertion NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_head.
- NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_assertion description "[Here we describe the construction and characterization of DNA libraries for the Langer-Giedion syndrome chromosome region (LGCR, 8q23-24.1), Wilms tumor chromosome region 1 (WT1, 11p13), Prader-Willi syndrome/Angelman syndrome chromosome region (PWCR/ANCR, 15q11.2-12), meningioma chromosome region (MGCR, 22q12-13), and fragile X chromosome region (FRAXA, Xq27.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_provenance.
- NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_assertion evidence source_evidence_literature NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_provenance.
- NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_assertion SIO_000772 2159949 NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_provenance.
- NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_assertion wasDerivedFrom befree-2016 NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_provenance.
- NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_assertion wasGeneratedBy ECO_0000203 NP895655.RATfTIo1gUItebPcXXFVXox5y3aUTReeLXNuzYdox5rPk130_provenance.