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- source_evidence_literature type ECO_0000212 NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_provenance.
- NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_assertion wasGeneratedBy ECO_0000203 NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_provenance.
- NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_assertion wasDerivedFrom befree-20140225 NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_provenance.
- NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_assertion SIO_000772 20358387 NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_provenance.
- NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_assertion evidence source_evidence_literature NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_provenance.
- NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_assertion description "[We have analyzed the somatic mutations in 89 cutaneous neurofibromas derived from three unrelated NF1 patients with high tumor burden, by loss of heterozygosity (LOH) analysis of the NF1, TP53, RB1, and CDKN2A genes, by assessing microsatellite instability (MSI), by direct sequencing of the NF1, TP53, and several mismatch repair (MMR) genes and by multiplex ligation-dependent probe amplification of the NF1 and TP53 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP743678.RAQEWt9Yp_L7yD3p5Rfbv52Glj0D4SgmSLSgIj-tgcQV8130_provenance.