Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_provenance.
- NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_assertion description "[A single nucleotide polymorphism in FGD4 was associated with the onset of sensory peripheral neuropathy in the discovery cohort [rs10771973; HR, 1.57; 95% confidence interval (CI), 1.30-1.91; P = 2.6 � 10(-6)] and in a European (HR, 1.72; 95% CI, 1.06-2.80; P = 0.013) and African American (HR, 1.93; 95% CI, 1.13-3.28; P = 6.7 � 10(-3)) replication cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_provenance.
- NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_assertion evidence source_evidence_literature NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_provenance.
- NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_assertion SIO_000772 22843789 NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_provenance.
- NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_assertion wasDerivedFrom befree-2016 NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_provenance.
- NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_assertion wasGeneratedBy ECO_0000203 NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1001236.RALejVVMx55SwS6GnEtGdbof2M8oAfZPF8Q30tVWwuHpE130_provenance.