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- NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_assertion type Assertion NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_head.
- NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_assertion description "[It usually occurs sporadically but familial cases are observed, with a subset of cases occurring in association with congenital malformations of the neural crest being linked to germline mutations of the PHOX2B gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_provenance.
- NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_assertion evidence source_evidence_literature NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_provenance.
- NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_assertion SIO_000772 18923523 NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_provenance.
- NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_assertion wasDerivedFrom befree-2016 NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_provenance.
- NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_assertion wasGeneratedBy ECO_0000203 NP698284.RAL2-mTAnHnujXeuvI6h9KXwQxzElsFiJ1Ga_IfFRvjJU130_provenance.