Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_provenance.
- NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_assertion description "[Five markers that reside within a 550?kb intergenic region on chromosome 13q33.3, between the MYO16 and IRS2 genes, also showed suggestive association with ASD in the MO families (p?=?3.3?�?10(-5) to 5.3?�?10(-7) ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_provenance.
- NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_assertion evidence source_evidence_literature NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_provenance.
- NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_assertion SIO_000772 24132906 NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_provenance.
- NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_assertion wasDerivedFrom befree-20150227 NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_provenance.
- NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_assertion wasGeneratedBy ECO_0000203 NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP801381.RAyam1cF61FxGnXvJHR6r3XVd8OHW5wwhC-qngJg0R59c130_provenance.