@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:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_head { this: np:hasAssertion dgn-np:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_assertion; np:hasProvenance dgn-np:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_provenance; np:hasPublicationInfo dgn-np:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_publicationInfo; a np:Nanopublication . dgn-np:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_assertion a np:Assertion . dgn-np:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_provenance a np:Provenance . dgn-np:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_publicationInfo a np:PublicationInfo . } dgn-np:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_assertion { miriam-gene:3075 a ncit:C16612 . lld:C0600518 a ncit:C7057 . dgn-gda:DGN30591cd11ba6599ca8e28018dc1f7627 sio:SIO_000628 miriam-gene:3075, lld:C0600518; a sio:SIO_001122 . } dgn-np:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_provenance { dgn-np:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_assertion dcterms:description "[In accordance with findings from the majority of previous study populations, the Tyr402His variant of CFH is associated with NVAMD in Israel. However, heterogeneity in clinical manifestations of NVAMD and in its response to PDT is not underlined by this C]. 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:18852870; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP104314.RAk4SkV1WYFv2sw4W4hcANTcqw4bB6_EkAkj_9VsBqCH4130_publicationInfo { this: dcterms:created "2015-08-25T14:38:37+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }