@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:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_head { this: np:hasAssertion dgn-np:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_assertion; np:hasProvenance dgn-np:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_provenance; np:hasPublicationInfo dgn-np:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_publicationInfo; a np:Nanopublication . dgn-np:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_assertion a np:Assertion . dgn-np:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_provenance a np:Provenance . dgn-np:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_publicationInfo a np:PublicationInfo . } dgn-np:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_assertion { miriam-gene:1285 a ncit:C16612 . lld:C1836876 a ncit:C7057 . dgn-gda:DGN5b91c16e96722dc7a0bf9df610216367 sio:SIO_000628 miriam-gene:1285, lld:C1836876; a sio:SIO_001121 . } dgn-np:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_provenance { dgn-np:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_assertion dcterms:description "[Genetic diseases affecting laminin and type IV collagen synthesis also are presented, with an emphasis on mutations to LAMB2 (Pierson syndrome) and COL4A3, COL4A4, and COL4A5 (Alport syndrome), and their experimental mouse models.]. 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:22958488; 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:NP1011179.RAhNDvK8jXQLbbDjZUJ6epA8n_wsBm1oI5MmQiDvco_HI130_publicationInfo { this: dcterms:created "2016-05-13T12:49:24+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" . }