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- source_evidence_literature type ECO_0000212 NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_provenance.
- NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_assertion description "[Mutations in the human TBX5 gene cause Holt-Oram syndrome (HOS), a disorder characterized by heart and upper limb deformities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_provenance.
- NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_assertion evidence source_evidence_literature NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_provenance.
- NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_assertion SIO_000772 15221798 NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_provenance.
- NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_assertion wasDerivedFrom befree-20150227 NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_provenance.
- NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_assertion wasGeneratedBy ECO_0000203 NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP724151.RA-YP1UOkBxt3opnmeq5Y5rAtVfaSQSCxgNfXs3VNsdWY130_provenance.