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- source_evidence_literature type ECO_0000212 NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_provenance.
- befree-2016 importedOn "2016-02-19" NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_provenance.
- NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_assertion wasGeneratedBy ECO_0000203 NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_provenance.
- NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_assertion wasDerivedFrom befree-2016 NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_provenance.
- NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_assertion SIO_000772 18948003 NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_provenance.
- NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_assertion evidence source_evidence_literature NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_provenance.
- NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_assertion description "[Mutations in C-terminal titin cause autosomal dominant tibial muscular dystrophy (TMD) as reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699523.RAOrgloSE_wqy3mZYpy19-5Njp-brYhUpvnvkFZ1FMnFA130_provenance.