Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_provenance.
- NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_assertion description "[HLA polymorphisms in Italian children with autism spectrum disorders: results of a family based linkage study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_provenance.
- NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_assertion evidence source_evidence_literature NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_provenance.
- NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_assertion SIO_000772 21084121 NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_provenance.
- NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_assertion wasDerivedFrom gad-20150221 NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_provenance.
- NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_assertion wasGeneratedBy ECO_0000203 NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_provenance.
- gad-20150221 importedOn "2015-02-21" NP188382.RAloPWHGRfGwcSb5g9IghlEcX9FI2K5VwHsSmrkP7Ax-c130_provenance.