Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_assertion type Assertion NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_head.
- NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_assertion wasGeneratedBy ECO_0000203 NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_provenance.
- NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_assertion wasDerivedFrom befree-20150227 NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_provenance.
- NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_assertion SIO_000772 23714752 NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_provenance.
- NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_assertion evidence source_evidence_literature NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_provenance.
- NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320100.RAf72EKw-240KV8ov5zYWXEkLu2eEg6l9-c43KlQe4COI130_provenance.