Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_provenance.
- NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_assertion description "[Haplotype results indicate that the minor allele of the rs4739217 is a risk factor for TD (permuted allelic p = 0.074). Age was also a risk factor for TD in our sample (p = 0.0001). Taken together, our findings suggest that GFRA2 genetic variants and age ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_provenance.
- NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_assertion evidence source_evidence_literature NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_provenance.
- NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_assertion SIO_000772 20369355 NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_provenance.
- NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_assertion wasDerivedFrom gad-20150221 NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_provenance.
- NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_assertion wasGeneratedBy ECO_0000203 NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_provenance.
- gad-20150221 importedOn "2015-02-21" NP169048.RA4ffWDHSoFQbBA4Lw78bam_xlSdmJA9fj3vmcT34IN2g130_provenance.