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- source_evidence_literature type ECO_0000212 NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_provenance.
- NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_assertion description "[A novel mutation in exon 8 of the PSEN1 gene (V261L) was associated with early-onset autosomal dominant Alzheimer's disease & spastic paraparesis in 3 family members.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_provenance.
- NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_assertion evidence source_evidence_literature NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_provenance.
- NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_assertion SIO_000772 18637955 NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_provenance.
- NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_assertion wasDerivedFrom lhgdn-20090331 NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_provenance.
- NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_assertion wasGeneratedBy ECO_0000203 NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP240179.RAvYEDVSx-pA76f6VRqjfb0icdjMDgT6Rm-E46TBHofBU130_provenance.