Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_provenance.
- NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_assertion description "[Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_provenance.
- NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_assertion evidence source_evidence_literature NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_provenance.
- NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_assertion SIO_000772 19068277 NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_provenance.
- NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_assertion wasDerivedFrom befree-20140225 NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_provenance.
- NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_assertion wasGeneratedBy ECO_0000203 NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP170385.RA9cEEP1RA4GJpZmkFxz2Z033eOOGM_DxU8Sk7VSVwDNk130_provenance.