Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_provenance.
- NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_assertion description "[Considering that there is overlap of the clinical manifestations and pathological characteristics between PD and MSA, we studied the possible associations between R1628P and G2385R polymorphisms of the LRRK2 and MSA in a population of Han Chinese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_provenance.
- NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_assertion evidence source_evidence_literature NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_provenance.
- NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_assertion SIO_000772 25511328 NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_provenance.
- NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_assertion wasDerivedFrom befree-2016 NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_provenance.
- NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_assertion wasGeneratedBy ECO_0000203 NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP1248327.RASvlvVgNVvi2LFrZvJGNFn6vI3gvXp1SeYk9IyeP_p3Q130_provenance.