@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:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_head { this: np:hasAssertion dgn-np:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_assertion; np:hasProvenance dgn-np:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_provenance; np:hasPublicationInfo dgn-np:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_publicationInfo; a np:Nanopublication . dgn-np:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_assertion a np:Assertion . dgn-np:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_provenance a np:Provenance . dgn-np:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_publicationInfo a np:PublicationInfo . } dgn-np:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_assertion { miriam-gene:720 a ncit:C16612 . lld:C0033626 a ncit:C7057 . dgn-gda:DGN3f809aae8a774f60d0371ac1547dd1c8 sio:SIO_000628 miriam-gene:720, lld:C0033626; a sio:SIO_001121 . } dgn-np:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_provenance { dgn-np:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_assertion dcterms:description "[To determine whether gene conversion at the C4A locus would encode a C4B-like protein and be responsible for the C4A protein deficiency (in nonDR3 patients), the C4d region of the gene was amplified by polymerase chain reaction and subjected to Nla IV digestion, and restriction fragment analysis was performed using a C4d region-specific probe.]. 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:2044237; 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:NP810078.RAojicZASwzDl6QepHKoeOQIk_Dxy2O8_Ft8fdaLaDWd4130_publicationInfo { this: dcterms:created "2016-05-13T12:47:52+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" . }