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- source_evidence_literature type ECO_0000212 NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_provenance.
- NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_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." NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_provenance.
- NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_assertion evidence source_evidence_literature NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_provenance.
- NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_assertion SIO_000772 19643772 NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_provenance.
- NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_assertion wasDerivedFrom befree-20140225 NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_provenance.
- NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_assertion wasGeneratedBy ECO_0000203 NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP450703.RAhEHfdk4U-Nrav63PE8OUAnEJ_kIX7ct2atuUsWdxvBY130_provenance.