Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_assertion type Assertion NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_head.
- NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_assertion wasGeneratedBy ECO_0000203 NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_provenance.
- NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_assertion wasDerivedFrom befree-20140225 NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_provenance.
- NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_assertion SIO_000772 15880323 NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_provenance.
- NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_assertion evidence source_evidence_literature NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_provenance.
- NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_assertion description "[It is unclear whether individuals with TBMN and impaired renal function represent part of the spectrum of TBMN associated with heterozygous COL4A3 or COL4A4 mutations, or if their disease is caused by mutations of other genes, or whether it is caused by a second coexistent renal lesion or is misdiagnosed Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476369.RAQO_xmm_eHi0eSVI2cUQethM6VJIzXHClWDqv9ZKJuPM130_provenance.