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- NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_assertion type Assertion NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_head.
- NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_assertion description "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_provenance.
- NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_assertion evidence source_evidence_literature NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_provenance.
- NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_assertion SIO_000772 23378035 NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_provenance.
- NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_assertion wasDerivedFrom befree-20150227 NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_provenance.
- NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_assertion wasGeneratedBy ECO_0000203 NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_provenance.