Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_provenance.
- NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_assertion description "[In 253 Gilman probable or definite MSA patients, 457 possible, probable, and definite MSA cases and 1472 controls, a frequency difference for the individual tagging SNPs or tag-defined haplotypes was not detected. No effect was observed of polymorphisms on the pathological expression of MSA in pathologically confirmed cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_provenance.
- NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_assertion evidence source_evidence_literature NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_provenance.
- NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_assertion SIO_000772 16543523 NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_provenance.
- NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_assertion wasDerivedFrom gad-20130706 NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_provenance.
- NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_assertion wasGeneratedBy ECO_0000203 NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP67555.RAVgyRWIR4NGV-fKhM_KWPQFAy27TgZPFWGcdNA-Zy8gI130_provenance.