Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_assertion> ?p ?o ?g. }
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- NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_assertion type Assertion NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_head.
- NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_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." NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_provenance.
- NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_assertion evidence source_evidence_literature NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_provenance.
- NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_assertion SIO_000772 18923523 NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_provenance.
- NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_assertion wasDerivedFrom befree-20150227 NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_provenance.
- NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_assertion wasGeneratedBy ECO_0000203 NP811465.RAqM5dSUCq_Y3IYAihJ3mbyw2U2fF7Yj8c26xIJ05OsVA130_provenance.