Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_provenance.
- NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_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." NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_provenance.
- NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_assertion evidence source_evidence_literature NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_provenance.
- NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_assertion SIO_000772 20590811 NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_provenance.
- NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_assertion wasDerivedFrom befree-20140225 NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_provenance.
- NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_assertion wasGeneratedBy ECO_0000203 NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316629.RA4L2MTkH8R7o9NW8dzhE8yxUBGijLDuU-ZntKxRYVl2s130_provenance.