Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_assertion> ?p ?o ?g. }
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- NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_assertion type Assertion NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_head.
- NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_assertion description "[The association was confirmed in an independent CAD case-control sample (CATHGEN) and strong association with MI was identified with single nucleotide polymorphisms (SNPs) in the 3' end of FAM5C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_provenance.
- NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_assertion evidence source_evidence_literature NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_provenance.
- NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_assertion SIO_000772 18430236 NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_provenance.
- NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_assertion wasDerivedFrom befree-20140225 NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_provenance.
- NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_assertion wasGeneratedBy ECO_0000203 NP835462.RAcLeuOPoSEHiE_UeIAJcZnQgRT1Gsq3uLd9f_NGaDn7A130_provenance.