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- NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_assertion type Assertion NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_head.
- NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_assertion description "[In 283, genetic mutation of EIF2B was confirmed with the onset of vanishing white matter disease reported as antenatal (seven), infantile (eight), early childhood (107), between infantile and early childhood (20), late childhood (25), between early and late childhood (three), adult (68), and between late childhood and adult (21).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_provenance.
- NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_assertion evidence source_evidence_literature NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_provenance.
- NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_assertion SIO_000772 24938145 NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_provenance.
- NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_assertion wasDerivedFrom befree-20150227 NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_provenance.
- NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_assertion wasGeneratedBy ECO_0000203 NP810429.RAaW6fMXeNA-JeMM-o7BY31852zr72RjnP-PVXY_qNL_s130_provenance.