Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_provenance.
- NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_assertion description "[Additional loci and genes (OPA2, OPA6 and OPA7) are responsible for X-linked or recessive optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_provenance.
- NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_assertion evidence source_evidence_literature NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_provenance.
- NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_assertion SIO_000772 22776096 NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_provenance.
- NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_assertion wasDerivedFrom befree-20140225 NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_provenance.
- NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_assertion wasGeneratedBy ECO_0000203 NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP473332.RAlEZ_SSzVu0w_h03-sEx0Vj4sE46SnYbgPZxOpO1VmHk130_provenance.