Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_provenance.
- NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_assertion wasGeneratedBy ECO_0000203 NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_provenance.
- NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_assertion wasDerivedFrom befree-20150227 NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_provenance.
- NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_assertion SIO_000772 25066065 NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_provenance.
- NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_assertion evidence source_evidence_literature NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_provenance.
- NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_assertion description "[PCD can be caused by hemizygous DNAH5 mutation in combination with a 5p segmental deletion attributable to CdCS on the opposite chromosome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356113.RARTJ6LnVN2ObpDt-6jdXFywzfuYINbqFsCn2xJ754BVQ130_provenance.