Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_provenance.
- NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_assertion description "[Mutations and variants in the cohesion factor genes NIPBL, SMC1A, and SMC3 in a cohort of 30 unrelated patients with Cornelia de Lange syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_provenance.
- NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_assertion evidence source_evidence_literature NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_provenance.
- NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_assertion SIO_000772 20358602 NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_provenance.
- NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_assertion wasDerivedFrom gad-20150221 NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_provenance.
- NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_assertion wasGeneratedBy ECO_0000203 NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP168848.RAVHPvrxUCt5XHala32cFpdIhoIL86phSe6bT_wAhhkFA130_provenance.