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- source_evidence_literature type ECO_0000212 NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_provenance.
- NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_assertion description "[Furthermore, we suggest that the diagnosis should be refined to, for example, NS-PTPN11-associated or CFC-BRAF-associated syndromes after the genetic defect has been established, as this may affect the prognosis and treatment of the patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_provenance.
- NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_assertion evidence source_evidence_literature NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_provenance.
- NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_assertion SIO_000772 18456719 NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_provenance.
- NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_assertion wasDerivedFrom befree-2016 NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_provenance.
- NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_assertion wasGeneratedBy ECO_0000203 NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_provenance.
- befree-2016 importedOn "2016-02-19" NP669367.RAhqMTVocPbNWb2_4mAJ-wy_jTb3K46zW-Ixst5sViGMY130_provenance.