Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_provenance.
- NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_assertion description "[Loci with distinct effects in the two diseases included INS on chromosome 11p15, IL2RA on chromosome 10p15, and PTPN22 on chromosome 1p13 in type 1 diabetes and IL12A on 3q25 and LPP on 3q28 in celiac disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_provenance.
- NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_assertion evidence source_evidence_literature NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_provenance.
- NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_assertion SIO_000772 19073967 NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_provenance.
- NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_assertion wasDerivedFrom befree-2016 NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_provenance.
- NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_assertion wasGeneratedBy ECO_0000203 NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_provenance.
- befree-2016 importedOn "2016-02-19" NP708467.RABiZRcIAyk7WWS3hUnklurfDEkFkcygOzPLEu3p6yRzE130_provenance.