Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_provenance.
- NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_assertion description "[Fatty acid hydroxylase-associated neurodegeneration due to fatty acid 2-hydroxylase deficiency presents with a wide range of phenotypes including spastic paraplegia, leukodystrophy, and/or brain iron deposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_provenance.
- NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_assertion evidence source_evidence_literature NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_provenance.
- NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_assertion SIO_000772 22146942 NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_provenance.
- NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_assertion wasDerivedFrom befree-20150227 NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_provenance.
- NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_assertion wasGeneratedBy ECO_0000203 NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP942852.RAp6xBYTjRHrA8f25o1QdolEII6YLL140iJ022Nx1BHL0130_provenance.