Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_assertion> ?p ?o ?g. }
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- NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_assertion type Assertion NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_head.
- NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_assertion description "[In contrast to the previously held belief that only 10% of cases had a genetic component, currently about one-third of all aPCA/eFPGL cases are thought to be attributable to germline mutations in at least nine genes (NF1, RET, SDHA, SDHB, SDHC, SDHD, TMEM127, MAX and VHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_provenance.
- NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_assertion evidence source_evidence_literature NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_provenance.
- NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_assertion SIO_000772 21896620 NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_provenance.
- NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_assertion wasDerivedFrom befree-2016 NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_provenance.
- NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_assertion wasGeneratedBy ECO_0000203 NP921713.RAac59BSfrjDL8Yo8fEHiwQW8WH4YvpvWIvqJL-VDOOK4130_provenance.