Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_assertion> ?p ?o ?g. }
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- NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_assertion type Assertion NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_head.
- NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_assertion description "[Twenty-one unrelated children with persistent familial hematuria as well as their families were studied for segregation of hematuria with haplotypes at the COL4A3/COL4A4 locus for benign familial hematuria and at the COL4A5 locus for X-linked Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_provenance.
- NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_assertion evidence source_evidence_literature NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_provenance.
- NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_assertion SIO_000772 16235097 NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_provenance.
- NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_assertion wasDerivedFrom befree-2016 NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_provenance.
- NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_assertion wasGeneratedBy ECO_0000203 NP518639.RAVSraVQv9gxaJ3MkoY__XBVNehxkeeFuh9DXNbKnSLfA130_provenance.