Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP820468.RAIyyTrTwJRtLe5_UQUtsNC2BeNVX41xsOLKfE9VmxLKs130_provenance.