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- source_evidence_literature type ECO_0000212 NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_provenance.
- NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_assertion description "[Barth syndrome (BTHS) is a genetic, X-linked, rare but often fatal, pediatric skeletal- and cardiomyopathy occurring due to mutations in the tafazzin gene (TAZ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_provenance.
- NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_assertion evidence source_evidence_literature NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_provenance.
- NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_assertion SIO_000772 25185984 NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_provenance.
- NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_assertion wasDerivedFrom befree-2016 NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_provenance.
- NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_assertion wasGeneratedBy ECO_0000203 NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216544.RAM8S7S1uEslxwPnGEXH3Zs-CRRedl_IsIxysrzew_ZFk130_provenance.