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- source_evidence_literature type ECO_0000212 NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_provenance.
- NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_assertion wasGeneratedBy ECO_0000203 NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_provenance.
- NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_assertion wasDerivedFrom befree-20150227 NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_provenance.
- NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_assertion SIO_000772 21965087 NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_provenance.
- NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_assertion evidence source_evidence_literature NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_provenance.
- NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_assertion description "[Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609568.RADAIpUB1ua0bYj-2VmT6YH_M4C-2Vdw1o_x4KWaJNTbs130_provenance.