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- source_evidence_literature type ECO_0000212 NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_provenance.
- NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_assertion description "[We report herein the first IRAP patients carrying the rare R104Q and D12E?TNFRSF1A gene mutations, thus expanding the spectrum of tumour necrosis factor receptor-1-associated periodic syndrome mutations in IRAP patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_provenance.
- NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_assertion evidence source_evidence_literature NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_provenance.
- NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_assertion SIO_000772 23745996 NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_provenance.
- NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_assertion wasDerivedFrom befree-20150227 NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_provenance.
- NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_assertion wasGeneratedBy ECO_0000203 NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP748103.RAhbLmKdahkE77lkuOCitUYi73yNzFe-U31vA27Br1GiA130_provenance.