Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_provenance.
- NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_assertion description "[Finding of alternative associating haplotypes in the same set of BPD families gives evidence for allelic heterogeneity within DISC1, eventually leading to heterogeneity in the clinical outcome as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_provenance.
- NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_assertion evidence source_evidence_literature NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_provenance.
- NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_assertion SIO_000772 17673452 NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_provenance.
- NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_assertion wasDerivedFrom befree-2016 NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_provenance.
- NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_assertion wasGeneratedBy ECO_0000203 NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_provenance.
- befree-2016 importedOn "2016-02-19" NP623380.RAvMBwd-9VVDSJ6acm8nLpyYMQz6gT1KIcgwlTMUGB4ts130_provenance.