Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_assertion> ?p ?o ?g. }
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- NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_assertion type Assertion NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_head.
- NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_assertion description "[In order to investigate the role of variation in NLR genes for AD, we genotyped 23 single nucleotide polymorphisms (SNPs) in seven selected NLR genes (CARD4, CARD15, CARD12, NALP1, NALP3, NALP12, MHC2TA) in 392 AD patients and 297 controls by restriction enzyme digestion or TaqMan assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_provenance.
- NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_assertion evidence source_evidence_literature NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_provenance.
- NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_assertion SIO_000772 17620097 NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_provenance.
- NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_assertion wasDerivedFrom befree-20150227 NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_provenance.
- NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_assertion wasGeneratedBy ECO_0000203 NP842238.RAU0KbzNPFYEq4jTT4PPAVWU5H63mb610sdXLj7JnHR7c130_provenance.