Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_assertion> ?p ?o ?g. }
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- NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_assertion type Assertion NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_head.
- NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_assertion description "[The SNPs (V4 G/C, T2 A/G, T1 G/A, and Q - 1A/G) of the ADAM33 gene may be the causal variants in ARA disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_provenance.
- NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_assertion evidence source_evidence_literature NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_provenance.
- NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_assertion SIO_000772 18752037 NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_provenance.
- NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_assertion wasDerivedFrom befree-20140225 NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_provenance.
- NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_assertion wasGeneratedBy ECO_0000203 NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_provenance.