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- source_evidence_literature type ECO_0000212 NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_provenance.
- NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_assertion description "[The position of the mutations and the loss of heterozygosity of MAP3K5 and MAP3K9 in 85% and 67% of melanoma samples, respectively, together suggest that the mutations are likely to be inactivating.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_provenance.
- NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_assertion evidence source_evidence_literature NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_provenance.
- NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_assertion SIO_000772 22197930 NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_provenance.
- NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_assertion wasDerivedFrom befree-20140225 NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_provenance.
- NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_assertion wasGeneratedBy ECO_0000203 NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_provenance.
- befree-20140225 importedOn "2014-02-25" NP768394.RA7f-CPdLJ0L3AirkQcq4U1VMPGAI9pyMnPKyrlUnFr78130_provenance.