Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_assertion type Assertion NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_head.
- NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_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." NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_provenance.
- NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_assertion evidence source_evidence_literature NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_provenance.
- NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_assertion SIO_000772 16235097 NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_provenance.
- NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_assertion wasDerivedFrom befree-2016 NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_provenance.
- NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_assertion wasGeneratedBy ECO_0000203 NP518645.RAdRAZa2j8mvA85jKm_kRABVitjUm60sS7O0AVmLv4KqQ130_provenance.