Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_assertion> ?p ?o ?g. }
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- NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_assertion type Assertion NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_head.
- NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_assertion description "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_provenance.
- NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_assertion evidence source_evidence_literature NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_provenance.
- NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_assertion SIO_000772 19194956 NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_provenance.
- NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_assertion wasDerivedFrom befree-20150227 NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_provenance.
- NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_assertion wasGeneratedBy ECO_0000203 NP873986.RA4CQFvyJwUMHUfezOSz1ZR_Ef9N9Vouph_AtTauHdKV0130_provenance.