Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_provenance.
- NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_assertion description "[To investigate the association of CASR variation in AD susceptibility, we genotyped a polymorphic dinucleotide repeat marker within intron 4, one SNP within the promoter region and three non-synonymous SNPs within exon 7 of the CASR gene and tested for association analysis, using a well-characterized cohort of AD cases (n = 692) and controls (n = 435).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_provenance.
- NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_assertion evidence source_evidence_literature NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_provenance.
- NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_assertion SIO_000772 19035514 NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_provenance.
- NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_assertion wasDerivedFrom gad-20130706 NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_provenance.
- NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_assertion wasGeneratedBy ECO_0000203 NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_provenance.
- gad-20130706 importedOn "2013-07-06" NP79150.RABA7S9PBm7VjeJ0zSAQI9M_9Cvq7vIX5tCERAUFTcnfc130_provenance.