@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:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_head { this: np:hasAssertion dgn-np:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_assertion; np:hasProvenance dgn-np:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_provenance; np:hasPublicationInfo dgn-np:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_publicationInfo; a np:Nanopublication . dgn-np:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_assertion a np:Assertion . dgn-np:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_provenance a np:Provenance . dgn-np:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_publicationInfo a np:PublicationInfo . } dgn-np:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_assertion { miriam-gene:3827 a ncit:C16612 . lld:C0030193 a ncit:C7057 . dgn-gda:DGNbf3841b32045c474c1357e043edc49e7 sio:SIO_000628 miriam-gene:3827, lld:C0030193; a sio:SIO_001121 . } dgn-np:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_provenance { dgn-np:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_assertion dcterms:description "[Increased understanding of the role of bradykinin in hereditary and acquired forms of C1 esterase inhibitor deficiency has led to the development of more targeted treatments for this painful, debilitating and potentially life-threatening disease.]. 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:22456031; 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:NP970878.RAw1KCMaDh5JUc3mk_FT72bOXtCIi4DmDokbi88mrlVKI130_publicationInfo { this: dcterms:created "2016-05-13T12:49:05+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" . }