@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_head { this: np:hasAssertion dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_assertion; np:hasProvenance dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_provenance; np:hasPublicationInfo dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_publicationInfo; a np:Nanopublication . dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_assertion a np:Assertion . dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_provenance a np:Provenance . dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_publicationInfo a np:PublicationInfo . } dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_assertion { miriam-gene:1278 a ncit:C16612 . lld:C0268358 a ncit:C7057 . dgn-gda:DGN712900177b6732e8b9f43aa7d0ce90db sio:SIO_000628 miriam-gene:1278, lld:C0268358; a sio:SIO_001121 . } dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_provenance { dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_assertion dcterms:description "[Unlike type I procollagen molecules synthesized by cells from most other infants with osteogenesis imperfecta type II which contain increased lysyl hydroxylation and hydroxylysyl glycosylation along the triple helical domain, the abnormal molecules synthesized by these cells are not overmodified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:3372508; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1301671.RAgj8_yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130_publicationInfo { this: dcterms:created "2016-05-13T12:51:36+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }