Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_provenance.
- befree-2016 importedOn "2016-02-19" NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_provenance.
- NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_assertion wasGeneratedBy ECO_0000203 NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_provenance.
- NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_assertion wasDerivedFrom befree-2016 NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_provenance.
- NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_assertion SIO_000772 17594340 NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_provenance.
- NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_assertion evidence source_evidence_literature NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_provenance.
- NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_assertion description "[Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617066.RALteYuHAdNpuzpCiUDaBFWbVFl3rAas5l7s6HzYAOhSo130_provenance.