Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_provenance.
- NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_assertion description "[Parkin (PARK2) gene mutations are the major cause of autosomal recessive parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_provenance.
- NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_assertion evidence source_evidence_literature NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_provenance.
- NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_assertion SIO_000772 18987353 NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_provenance.
- NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_assertion wasDerivedFrom befree-20150227 NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_provenance.
- NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_assertion wasGeneratedBy ECO_0000203 NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_provenance.
- befree-20150227 importedOn "2015-02-27" NP608872.RAS0RPhjYzTKOVpXwmhJrgf3-p8fHl4tXW_ikDO-ZoPns130_provenance.