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- NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_assertion type Assertion NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_head.
- NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_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." NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_provenance.
- NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_assertion evidence source_evidence_literature NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_provenance.
- NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_assertion SIO_000772 18192287 NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_provenance.
- NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_assertion wasDerivedFrom befree-20140225 NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_provenance.
- NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_assertion wasGeneratedBy ECO_0000203 NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_provenance.