Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_provenance.
- NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_assertion description "[This contrasts with homozygous parkin, PINK1 or DJ1 parkinsonism, characterized by young-onset (usually <40 years), and a comparatively benign course of predominantly levodopa-responsive symptoms without dementia or prominent dysautonomia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_provenance.
- NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_assertion evidence source_evidence_literature NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_provenance.
- NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_assertion SIO_000772 19815446 NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_provenance.
- NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_assertion wasDerivedFrom befree-20140225 NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_provenance.
- NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_assertion wasGeneratedBy ECO_0000203 NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP900695.RAL4VpB1SPezOopRx9s06tfP8CxykEf6Rr9HzVt9z9pDM130_provenance.