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- source_evidence_literature type ECO_0000212 NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_provenance.
- NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_assertion description "[To identify common genetic variation contributing to risk for tauopathies, we carried out a genome-wide association study of 1,114 individuals with PSP (cases) and 3,247 controls (stage 1) followed by a second stage in which we genotyped 1,051 cases and 3,560 controls for the stage 1 SNPs that yielded P ? 10(-3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_provenance.
- NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_assertion evidence source_evidence_literature NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_provenance.
- NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_assertion SIO_000772 21685912 NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_provenance.
- NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_assertion wasDerivedFrom befree-20140225 NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_provenance.
- NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_assertion wasGeneratedBy ECO_0000203 NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP935541.RAfYl9BsKmz9No14-0g0m4pL9rT5lMNOlG-xnLiT7eIHg130_provenance.