Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_assertion> ?p ?o ?g. }
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- NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_assertion type Assertion NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_head.
- NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_assertion description "[This syndrome is caused by germline mutations in succinate dehydrogenase B (SDHB), C (SDHC), or D (SDHD) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_provenance.
- NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_assertion evidence source_evidence_literature NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_provenance.
- NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_assertion SIO_000772 19576851 NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_provenance.
- NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_assertion wasDerivedFrom gad-20150221 NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_provenance.
- NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_assertion wasGeneratedBy ECO_0000203 NP150112.RAhsUZtosZHo0c7v-W4O10pfG-k1-7SW-weDhEsCFWu70130_provenance.