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- source_evidence_literature type ECO_0000212 NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_provenance.
- NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_assertion description "[Germline mutations in the NKX2-5, GATA4, and CRELD1 genes do not appear to be associated with CHD in Mexican DS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_provenance.
- NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_assertion evidence source_evidence_literature NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_provenance.
- NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_assertion SIO_000772 25524324 NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_provenance.
- NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_assertion wasDerivedFrom befree-2016 NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_provenance.
- NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_assertion wasGeneratedBy ECO_0000203 NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249431.RAkXlz7Iaw1k_MHpPU88PlIf_a16Zxe87gvzUtg70UTS0130_provenance.