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- source_evidence_literature type ECO_0000212 NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_provenance.
- NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_assertion description "[About 60% of Pheochromocytoma (PCC) and Paraganglioma (PGL) patients have either germline or somatic mutations in one of the 12 proposed disease causing genes; SDHA, SDHB, SDHC, SDHD, SDHAF2, VHL, EPAS1, RET, NF1, TMEM127, MAX and H-RAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_provenance.
- NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_assertion evidence source_evidence_literature NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_provenance.
- NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_assertion SIO_000772 24466223 NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_provenance.
- NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_assertion wasDerivedFrom befree-20150227 NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_provenance.
- NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_assertion wasGeneratedBy ECO_0000203 NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_provenance.