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- source_evidence_literature type ECO_0000212 NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_provenance.
- NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_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." NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_provenance.
- NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_assertion evidence source_evidence_literature NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_provenance.
- NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_assertion SIO_000772 24132906 NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_provenance.
- NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_assertion wasDerivedFrom befree-20150227 NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_provenance.
- NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_assertion wasGeneratedBy ECO_0000203 NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP867057.RAUx0Fv_h6TZhF_Rrku6TkHszF78Kzt1o6IkN2M_c85Uw130_provenance.