Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion> ?p ?o ?g. }
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- NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion type Assertion NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_head.
- NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion description "[Thirteen unrelated children with TBMN and five individuals with autosomal recessive Alport syndrome were examined for mutations in the 52 exons of COL4A3 and the 47 coding exons of COL4A4 using single-stranded conformation polymorphism (SSCP) analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_provenance.
- NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion evidence source_evidence_literature NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_provenance.
- NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion SIO_000772 17216251 NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_provenance.
- NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion wasDerivedFrom befree-20150227 NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_provenance.
- NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_assertion wasGeneratedBy ECO_0000203 NP319895.RACB8vf9wu10Y6Z0isd0JZY9gXXKMTCIvR3Ce-3WIyuZk130_provenance.