Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_assertion> ?p ?o ?g. }
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- NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_assertion type Assertion NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_head.
- NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_assertion description "[COL4A1 may be a candidate gene in unexplained familial syndromes with autosomal dominant hematuria, cystic kidney disease, intracranial aneurysms, and muscle cramps.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_provenance.
- NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_assertion evidence source_evidence_literature NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_provenance.
- NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_assertion SIO_000772 18160688 NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_provenance.
- NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_assertion wasDerivedFrom lhgdn-20090331 NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_provenance.
- NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_assertion wasGeneratedBy ECO_0000203 NP213793.RA2Qa6P6m73gP5rxMRG4FAuIMRFOdKJquyWn4k3YzOxWI130_provenance.