Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_provenance.
- NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_assertion description "[While gross neuropathological changes are absent in most primary dystonias, including the paroxysmal forms, striking morphological alterations are found in some, such as in the X-linked dystonia-parkinsonism syndrome (DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_provenance.
- NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_assertion evidence source_evidence_literature NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_provenance.
- NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_assertion SIO_000772 19578124 NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_provenance.
- NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_assertion wasDerivedFrom befree-20140225 NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_provenance.
- NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_assertion wasGeneratedBy ECO_0000203 NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP711028.RAa4uMt9k1xn5c6NDl8hqKe3f79lGkwcMkQVJF6K5C0Zc130_provenance.