Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_provenance.
- NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_assertion description "[This review focuses on the eight monogenic primary dystonias, six of which are associated with an early-onset generalized phenotype (DYT1, 2, 4, 6, 16 and 17), while the remaining two are characterized by an adolescent- or adult-onset focal or segmental form of dystonia (DYT7 and 13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_provenance.
- NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_assertion evidence source_evidence_literature NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_provenance.
- NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_assertion SIO_000772 20590811 NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_provenance.
- NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_assertion wasDerivedFrom befree-20140225 NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_provenance.
- NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_assertion wasGeneratedBy ECO_0000203 NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP573079.RAi8FH1frodNl2H4KO4GNnlG5MKsBb2t6FlPmRy8XmGZc130_provenance.