Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_provenance.
- NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_assertion description "[Likewise, haplotype DRB1*04 is characterized in 1b-IDDM patients by a lower frequency of alleles TAP1-C (4.0%) and TAP2-B (8.0%) than in 1a-IDDM patients (22.2% and 25.9%, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_provenance.
- NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_assertion evidence source_evidence_literature NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_provenance.
- NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_assertion SIO_000772 8988536 NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_provenance.
- NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_assertion wasDerivedFrom befree-2016 NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_provenance.
- NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_assertion wasGeneratedBy ECO_0000203 NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1365374.RA-o9Z9XjOhSiMVhUFbS0KingZk7SsZ808_vVLg_mnj_s130_provenance.