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- source_evidence_literature type ECO_0000212 NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance.
- NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_assertion description "[Two hundred and twenty-three consecutive patients fulfilling clinical diagnostic criteria for frontotemporal lobar degeneration (FTLD), and 259 patients with motor neuron disease (MND), for whom genomic DNA was available, were investigated for the presence of mutations in tau (MAPT) and progranulin (PGRN) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance.
- NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_assertion evidence source_evidence_literature NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance.
- NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_assertion SIO_000772 18192287 NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance.
- NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_assertion wasDerivedFrom befree-20140225 NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance.
- NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_assertion wasGeneratedBy ECO_0000203 NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance.
- befree-20140225 importedOn "2014-02-25" NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance.