@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:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_head { this: np:hasAssertion dgn-np:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_assertion; np:hasProvenance dgn-np:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_provenance; np:hasPublicationInfo dgn-np:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_publicationInfo; a np:Nanopublication . dgn-np:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_assertion a np:Assertion . dgn-np:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_provenance a np:Provenance . dgn-np:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_publicationInfo a np:PublicationInfo . } dgn-np:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_assertion { miriam-gene:5310 a ncit:C16612 . lld:C0085413 a ncit:C7057 . dgn-gda:DGNde4e54254594a0b6a76c82d59a948021 sio:SIO_000628 miriam-gene:5310, lld:C0085413; a sio:SIO_001121 . } dgn-np:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_provenance { dgn-np:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_assertion dcterms:description "[Assuming that a clinic population represents the most severe forms of a disease and non PKD-1 is a less aggressive phenotype, the degree of genetic heterogeneity for APKD in the population may well be much greater than at present suggested.]. 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:8261645; 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:NP1337023.RAaHuNqBkYucUXAmGMR1Z0w4xBR6opwuA8Zi_ei1v18Cw130_publicationInfo { this: dcterms:created "2016-05-13T12:51:52+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" . }