Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance.
- NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance.
- NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_assertion evidence source_evidence_literature NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance.
- NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_assertion SIO_000772 20857310 NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance.
- NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_assertion wasDerivedFrom befree-20150227 NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance.
- NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_assertion wasGeneratedBy ECO_0000203 NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP920881.RAZf2IKV0sn0nle-n7573Vm0LCW1WQBp5vqVfpf5RzxGw130_provenance.