@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:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_head { this: np:hasAssertion dgn-np:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_assertion; np:hasProvenance dgn-np:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_provenance; np:hasPublicationInfo dgn-np:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_publicationInfo; a np:Nanopublication . dgn-np:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_assertion a np:Assertion . dgn-np:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_provenance a np:Provenance . dgn-np:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_publicationInfo a np:PublicationInfo . } dgn-np:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_assertion { miriam-gene:6690 a ncit:C16612 . lld:C0001339 a ncit:C7057 . dgn-gda:DGNcbc284922f93d7cb734097c3f683d1cd sio:SIO_000628 miriam-gene:6690, lld:C0001339; a sio:SIO_001122 . } dgn-np:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_provenance { dgn-np:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_assertion dcterms:description "[The p.N34S mutation in SPINK1 gene was found more frequently in patients with AP in the Indian population, irrespective of disease etiology and whether the disease was recurrent or not, and was associated with disease onset at an earlier age.]. 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:24844923; 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:NP1184067.RAvc4z8YzZ6zqD9NV54HjcGZCG2bi9hZO7Qhs_c-57A0k130_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" . }