Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_provenance.
- NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_assertion description "[The family's Brown syndrome trait was analyzed for linkage to the known congenital fibrosis syndrome loci and the CFEOM2 gene, ARIX, was sequenced in affected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_provenance.
- NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_assertion evidence source_evidence_literature NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_provenance.
- NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_assertion SIO_000772 12324876 NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_provenance.
- NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_assertion wasDerivedFrom befree-2016 NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_provenance.
- NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_assertion wasGeneratedBy ECO_0000203 NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_provenance.
- befree-2016 importedOn "2016-02-19" NP368868.RAfdE-Geh6Z8WXBJtxsgINv-zeQ0LgSbyIdw-dzqSNbgc130_provenance.