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- source_evidence_literature type ECO_0000212 NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_provenance.
- NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_assertion description "[Conversely, the phenotype associated with TUBB4A mutations expanded from that of isolated dystonia to a syndrome of hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_provenance.
- NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_assertion evidence source_evidence_literature NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_provenance.
- NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_assertion SIO_000772 25643588 NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_provenance.
- NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_assertion wasDerivedFrom befree-2016 NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_provenance.
- NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_assertion wasGeneratedBy ECO_0000203 NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260239.RAR2ZwbthaXB_sQUsgMmslwSfMQCAizJSi6scgUjyn5Ao130_provenance.