Matches in DBpedia 2015-10 for { <http://doi.org/10.1186/1750-1172-8-100> ?p ?o }
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- 1750-1172-8-100 author1 "Wen".
- 1750-1172-8-100 doi "10.1186/1750-1172-8-100".
- 1750-1172-8-100 first1 "J".
- 1750-1172-8-100 first10 "B".
- 1750-1172-8-100 first11 "S".
- 1750-1172-8-100 first12 "N".
- 1750-1172-8-100 first13 "P".
- 1750-1172-8-100 first14 "E".
- 1750-1172-8-100 first2 "F".
- 1750-1172-8-100 first3 "G".
- 1750-1172-8-100 first4 "S. A.".
- 1750-1172-8-100 first5 "C".
- 1750-1172-8-100 first6 "Y".
- 1750-1172-8-100 first7 "S".
- 1750-1172-8-100 first8 "C".
- 1750-1172-8-100 first9 "C".
- 1750-1172-8-100 isCitedBy Exocyst_complex_component_6b.
- 1750-1172-8-100 journal "Orphanet Journal of Rare Diseases".
- 1750-1172-8-100 last10 "Ylstra".
- 1750-1172-8-100 last11 "Lewis".
- 1750-1172-8-100 last12 "Isoherranen".
- 1750-1172-8-100 last13 "MacIel".
- 1750-1172-8-100 last14 "Rajcan-Separovic".
- 1750-1172-8-100 last2 "Lopes".
- 1750-1172-8-100 last3 "Soares".
- 1750-1172-8-100 last4 "Farrell".
- 1750-1172-8-100 last5 "Nelson".
- 1750-1172-8-100 last6 "Qiao".
- 1750-1172-8-100 last7 "Martell".
- 1750-1172-8-100 last8 "Badukke".
- 1750-1172-8-100 last9 "Bessa".
- 1750-1172-8-100 pages "100".
- 1750-1172-8-100 pmc "3710273".
- 1750-1172-8-100 pmid "23837398".
- 1750-1172-8-100 title "Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2".
- 1750-1172-8-100 volume "8".
- 1750-1172-8-100 year "2013".