Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_provenance.
- NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_assertion description "[To determine the relative contribution of ZIC3 mutations to both heterotaxy and isolated CHD, we screened the coding region of ZIC3 in 194 unrelated patients, including 61 patients with classic heterotaxy, 93 patients with heart defects characteristic of heterotaxy, and 11 patients with situs inversus totalis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_provenance.
- NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_assertion evidence source_evidence_literature NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_provenance.
- NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_assertion SIO_000772 14681828 NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_provenance.
- NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_assertion wasDerivedFrom befree-20140225 NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_provenance.
- NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_assertion wasGeneratedBy ECO_0000203 NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP492692.RA6ysWvFABlWsHNwwohFYbrHFBQjRXC01nDRBg53ImRRY130_provenance.