Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_assertion type Assertion NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_head.
- NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_assertion description "[The H syndrome is caused by mutations in the nucleoside transporter hENT3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_provenance.
- NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_assertion evidence source_evidence_literature NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_provenance.
- NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_assertion SIO_000772 18940313 NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_provenance.
- NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_assertion wasDerivedFrom befree-2016 NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_provenance.
- NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_assertion wasGeneratedBy ECO_0000203 NP699174.RAfYdx3R-2v8BgPCOoOgOPEocqO0xpXLjHiwFPSk_-gWU130_provenance.