Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_provenance.
- NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_assertion description "[These results support the hypothesis that haplotype-specific variation in the MAPT 3' UTR underlies an A?-independent mechanism for neurodegeneration in TPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_provenance.
- NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_assertion evidence source_evidence_literature NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_provenance.
- NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_assertion SIO_000772 22802095 NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_provenance.
- NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_assertion wasDerivedFrom befree-20140225 NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_provenance.
- NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_assertion wasGeneratedBy ECO_0000203 NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP914728.RASDV8JoGFANdOLO-5V_Athi-CWYd3LLlyq7m1fw430T4130_provenance.