Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_assertion> ?p ?o ?g. }
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- NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_assertion type Assertion NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_head.
- NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_assertion description "[Ocular albinism type 1 (OA1) is an X-linked recessive disorder characterized by a major impairment of visual acuity, nystagmus, strabismus, photophobia and retinal hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_provenance.
- NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_assertion evidence source_evidence_literature NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_provenance.
- NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_assertion SIO_000772 7795590 NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_provenance.
- NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_assertion wasDerivedFrom befree-20140225 NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_provenance.
- NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_assertion wasGeneratedBy ECO_0000203 NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_provenance.