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- source_evidence_literature type ECO_0000212 NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_provenance.
- NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_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." NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_provenance.
- NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_assertion evidence source_evidence_literature NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_provenance.
- NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_assertion SIO_000772 19205068 NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_provenance.
- NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_assertion wasDerivedFrom gad-20150221 NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_provenance.
- NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_assertion wasGeneratedBy ECO_0000203 NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP140664.RASehwsSjbT4BH9cTdf_gA6EPEKSrRYAr4PeSeWdUrnV0130_provenance.