Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_provenance.
- NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_assertion description "[Other entities entailing dystonia-parkinsonism include dopamine transporter deficiency syndrome (SLC63 mutations); dopa-responsive dystonias; young-onset parkinsonism (PARKIN, PINK1 and DJ-1 mutations); PRKRA mutations; and X-linked TAF1 mutations, which rarely can also manifest in women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_provenance.
- NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_assertion evidence source_evidence_literature NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_provenance.
- NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_assertion SIO_000772 25643588 NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_provenance.
- NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_assertion wasDerivedFrom befree-2016 NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_provenance.
- NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_assertion wasGeneratedBy ECO_0000203 NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260248.RAaoVz4ldtgDP14FB9CYj8xV4d3USQgYMHJYjWSxkzjzA130_provenance.