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- source_evidence_literature type ECO_0000212 NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_provenance.
- NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_assertion description "[Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_provenance.
- NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_assertion evidence source_evidence_literature NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_provenance.
- NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_assertion SIO_000772 8931575 NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_provenance.
- NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_assertion wasDerivedFrom befree-2016 NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_provenance.
- NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_assertion wasGeneratedBy ECO_0000203 NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1362928.RAXkV_SQ_4fcB6ShL7HPyN4XwXkxq5tPMr81AX2nY9VtU130_provenance.