Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_provenance.
- NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_assertion description "[Using a molecular approach, we investigated SCA6 as well as other SCA subtype in 120 Mainland Chinese families with dominantly inherited ataxias and in 60 Mainland Chinese patients with sporadic ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_provenance.
- NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_assertion evidence source_evidence_literature NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_provenance.
- NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_assertion SIO_000772 15979648 NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_provenance.
- NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_assertion wasDerivedFrom befree-2016 NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_provenance.
- NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_assertion wasGeneratedBy ECO_0000203 NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_provenance.
- befree-2016 importedOn "2016-02-19" NP500986.RAvzJ_0CSR_OGJ4KQ2NCMpRjGtSX2UO2InGP9bReoqG88130_provenance.