Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_assertion> ?p ?o ?g. }
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- NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_assertion type Assertion NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_head.
- NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_assertion description "[Achondroplasia (ACH) is the most common form of osteochondrodysplasia, and is mostly associated with a point mutation in the gene on the transmembrane domain of fibroblast growth factor receptor-3 (FGFR-3) on chromosome 4p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_provenance.
- NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_assertion evidence source_evidence_literature NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_provenance.
- NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_assertion SIO_000772 9745773 NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_provenance.
- NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_assertion wasDerivedFrom befree-2016 NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_provenance.
- NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_assertion wasGeneratedBy ECO_0000203 NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_provenance.