Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_assertion> ?p ?o ?g. }
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- NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_assertion type Assertion NP546706.RAeo0T2igAn8T17SRpg74SXypBhFAOJaW3PztSo_GYNp8130_head.
- 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.