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- source_evidence_literature type ECO_0000212 NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_provenance.
- NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_assertion description "[These include lamin A/C in autosomal dominant Emery-Dreifuss muscular dystrophy, SMN in spinal muscular atrophy, SIX5 in myotonic dystrophy, calpain3 in type 2A limb-girdle muscular dystrophy, PABP2 in oculopharyngeal dystrophy, androgen receptor in spinal and bulbar muscular atrophy and the ataxins in hereditary ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_provenance.
- NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_assertion evidence source_evidence_literature NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_provenance.
- NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_assertion SIO_000772 10838245 NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_provenance.
- NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_assertion wasDerivedFrom befree-20140225 NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_provenance.
- NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_assertion wasGeneratedBy ECO_0000203 NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP390460.RA-Ui0hPwuv84Ls_V71lKxGQdglZhSqZkA1SjJCGysd2E130_provenance.