Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP191924.RAaxovB2XR3rriKAA2PkGzCn-HB2EQiVgvZAQC9-21R1g130_provenance.