Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_assertion> ?p ?o ?g. }
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- NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_assertion type Assertion NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_head.
- NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_provenance.
- NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_assertion evidence source_evidence_literature NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_provenance.
- NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_assertion SIO_000772 19643772 NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_provenance.
- NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_assertion wasDerivedFrom befree-20140225 NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_provenance.
- NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_assertion wasGeneratedBy ECO_0000203 NP661541.RA8MVgjRPEmSwsMFahP4uBnfd-HZZnWtpZAvQm_tYjJug130_provenance.