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- source_evidence_literature type ECO_0000212 NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_provenance.
- NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_assertion description "[(Nature 352, 539-540) demonstrated that the GLI3 gene in 7p13 was disrupted in, patients with Greig syndrome and, more recently, the linkage of genetic markers from 7p with the Saethre-Chotzen syndrome locus has been reported (2,3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_provenance.
- NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_assertion evidence source_evidence_literature NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_provenance.
- NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_assertion SIO_000772 7987323 NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_provenance.
- NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_assertion wasDerivedFrom befree-20150227 NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_provenance.
- NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_assertion wasGeneratedBy ECO_0000203 NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP428552.RAhrj-m-knMafawW87Ddmnr9Hqr3GOjxWHdBGu9kc1m6s130_provenance.