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dcterms:bibliographicCitation <http://dblp.uni-trier.de/rec/bibtex/journals/cbm/KumarBHVSGYZD22>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Ambritha_Balasundaram>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/C._George_Priya_Doss>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Cathryn_R._Hephzibah>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Gnanasambandan_Ramanathan>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Hatem_Zayed>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/R._Siva>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Rinku_Polachirakkal_Varghese>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/S._Udhaya_Kumar>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Salma_Younes>
foaf:homepage <http://dx.doi.org/doi.org%2F10.1016%2Fj.compbiomed.2022.105701>
foaf:homepage <https://doi.org/10.1016/j.compbiomed.2022.105701>
dc:identifier DBLP journals/cbm/KumarBHVSGYZD22 (xsd:string)
dc:identifier DOI doi.org%2F10.1016%2Fj.compbiomed.2022.105701 (xsd:string)
dcterms:issued 2022 (xsd:gYear)
swrc:journal <https://dblp.l3s.de/d2r/resource/journals/cbm>
rdfs:label Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes. (xsd:string)
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Ambritha_Balasundaram>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/C._George_Priya_Doss>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Cathryn_R._Hephzibah>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Gnanasambandan_Ramanathan>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Hatem_Zayed>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/R._Siva>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Rinku_Polachirakkal_Varghese>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/S._Udhaya_Kumar>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Salma_Younes>
swrc:pages 105701 (xsd:string)
owl:sameAs <http://bibsonomy.org/uri/bibtexkey/journals/cbm/KumarBHVSGYZD22/dblp>
owl:sameAs <http://dblp.rkbexplorer.com/id/journals/cbm/KumarBHVSGYZD22>
rdfs:seeAlso <http://dblp.uni-trier.de/db/journals/cbm/cbm148.html#KumarBHVSGYZD22>
rdfs:seeAlso <https://doi.org/10.1016/j.compbiomed.2022.105701>
dc:title Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes. (xsd:string)
dc:type <http://purl.org/dc/dcmitype/Text>
rdf:type swrc:Article
rdf:type foaf:Document
swrc:volume 148 (xsd:string)