Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_provenance.
- NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_assertion wasGeneratedBy ECO_0000203 NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_provenance.
- NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_assertion wasDerivedFrom befree-20150227 NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_provenance.
- NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_assertion SIO_000772 15001591 NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_provenance.
- NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_assertion evidence source_evidence_literature NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_provenance.
- NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_assertion description "[Clinical features in the remaining 11 cases with no demonstrable KAL1 or FGFR1 mutations included right renal aplasia in one female, cleft palate in one male, cleft palate and perceptive deafness in one male, and dental agenesis and perceptive deafness in one male, in addition to a variable extent of HH and olfactory dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400696.RAIoEdiVdyAfoDU9t3qseyS0U8rcs0cEigwXqwKkGN4qg130_provenance.