Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_provenance.
- NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_assertion wasGeneratedBy ECO_0000203 NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_provenance.
- NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_assertion wasDerivedFrom gad-20150221 NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_provenance.
- NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_assertion SIO_000772 12853230 NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_provenance.
- NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_assertion evidence source_evidence_literature NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_provenance.
- NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_assertion description "[We conclude that SCA-17 repeat expansion mutations are not a common cause of familial parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80588.RAaLZjlM7XqEFEtRYC7w3V-CXyXLpfLG_LZQffMJK6IEc130_provenance.