Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_provenance.
- NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_assertion description "[Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_provenance.
- NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_assertion evidence source_evidence_literature NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_provenance.
- NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_assertion SIO_000772 19205068 NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_provenance.
- NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_assertion wasDerivedFrom gad-20150221 NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_provenance.
- NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_assertion wasGeneratedBy ECO_0000203 NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_provenance.
- gad-20150221 importedOn "2015-02-21" NP140665.RA3tWLcrkv47N03COGjDie1UKlCMbKtKpVI0_HsSYD054130_provenance.