@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:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_head { this: np:hasAssertion dgn-np:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_assertion; np:hasProvenance dgn-np:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_provenance; np:hasPublicationInfo dgn-np:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_publicationInfo; a np:Nanopublication . dgn-np:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_assertion a np:Assertion . dgn-np:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_provenance a np:Provenance . dgn-np:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_publicationInfo a np:PublicationInfo . } dgn-np:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_assertion { miriam-gene:945 a ncit:C16612 . lld:C0004096 a ncit:C7057 . dgn-gda:DGNfac9d565291d6e06a27fe332439bbd09 sio:SIO_000628 miriam-gene:945, lld:C0004096; a sio:SIO_001121 . } dgn-np:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_provenance { dgn-np:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_assertion dcterms:description "[Leading examples, such as the CD33 polymorphism associated with late-onset Alzheimer's disease, are well supported by genetic replication and mechanistic studies, while some others (such as SIGLEC8 polymorphism associated with bronchial asthma and SIGLEC14 polymorphism associated with exacerbation of chronic obstructive pulmonary disease) may benefit reinforcement by independent genetic replication or mechanistic studies.]. 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:24841380; 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:NP1183744.RAnx4qdkHWSGicLrCIeZKhbX9Xj2Q7DFZNm9exj2ANMv4130_publicationInfo { this: dcterms:created "2016-05-13T12:50:42+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" . }