Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_assertion> ?p ?o ?g. }
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- NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_assertion type Assertion NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_head.
- NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_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." NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_provenance.
- NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_assertion evidence source_evidence_literature NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_provenance.
- NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_assertion SIO_000772 19643772 NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_provenance.
- NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_assertion wasDerivedFrom befree-20140225 NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_provenance.
- NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_assertion wasGeneratedBy ECO_0000203 NP540011.RAGigxp7uHTTaHRXxEilrzrfgaX-x_TDqntxERccjvW5k130_provenance.