Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_assertion type Assertion NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_head.
- NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_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." NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_provenance.
- NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_assertion evidence source_evidence_literature NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_provenance.
- NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_assertion SIO_000772 16235097 NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_provenance.
- NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_assertion wasDerivedFrom befree-20140225 NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_provenance.
- NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_assertion wasGeneratedBy ECO_0000203 NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_provenance.