[RDF data]
Home | Example Publications
PropertyValue
dcterms:bibliographicCitation <http://dblp.uni-trier.de/rec/bibtex/journals/biodb/YangYLCCLSS20>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Bairong_Shen>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Lan_Yang>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Xingyun_Liu>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Yalan_Chen>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Yan_Sun>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Yang_Yang>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Yongquan_Chen>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Yuxin_Lin>
foaf:homepage <http://dx.doi.org/doi.org%2F10.1093%2Fdatabase%2Fbaaa048>
foaf:homepage <https://doi.org/10.1093/database/baaa048>
dc:identifier DBLP journals/biodb/YangYLCCLSS20 (xsd:string)
dc:identifier DOI doi.org%2F10.1093%2Fdatabase%2Fbaaa048 (xsd:string)
dcterms:issued 2020 (xsd:gYear)
swrc:journal <https://dblp.l3s.de/d2r/resource/journals/biodb>
rdfs:label CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease. (xsd:string)
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Bairong_Shen>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Lan_Yang>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Xingyun_Liu>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Yalan_Chen>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Yan_Sun>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Yang_Yang>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Yongquan_Chen>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Yuxin_Lin>
owl:sameAs <http://bibsonomy.org/uri/bibtexkey/journals/biodb/YangYLCCLSS20/dblp>
owl:sameAs <http://dblp.rkbexplorer.com/id/journals/biodb/YangYLCCLSS20>
rdfs:seeAlso <http://dblp.uni-trier.de/db/journals/biodb/biodb2020.html#YangYLCCLSS20>
rdfs:seeAlso <https://doi.org/10.1093/database/baaa048>
dc:title CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease. (xsd:string)
dc:type <http://purl.org/dc/dcmitype/Text>
rdf:type swrc:Article
rdf:type foaf:Document
swrc:volume 2020 (xsd:string)