@prefix bfo: .
@prefix this: .
@prefix rdfs: .
@prefix xsd: .
@prefix sio: .
@prefix ncit: .
@prefix lld: .
@prefix miriam-gene: .
@prefix miriam-pubmed: .
@prefix wi: .
@prefix prov: .
@prefix pav: .
@prefix prv: .
@prefix dcterms: .
@prefix np: .
@prefix dgn-np: .
@prefix dgn-gda: .
@prefix dgn-void: .
dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_head {
this: np:hasAssertion dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_assertion;
np:hasProvenance dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_provenance;
np:hasPublicationInfo dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_publicationInfo;
a np:Nanopublication .
dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_assertion a np:Assertion .
dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_provenance a np:Provenance .
dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_publicationInfo a
np:PublicationInfo .
}
dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_assertion {
miriam-gene:8513 a ncit:C16612 .
lld:C0043208 a ncit:C7057 .
dgn-gda:DGNb7bde7ca75c832fb3651cc6201d81888 sio:SIO_000628 miriam-gene:8513, lld:C0043208;
a sio:SIO_001121 .
}
dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_provenance {
dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_assertion dcterms:description
"[RFLP and DNA sequence analysis revealed that they were heteroallelic for the common G(934)-->A substitution in exon 8 of the hLAL gene and a mutation which, if inherited on both alleles, would be expected to result in complete loss of enzyme activity and to cause Wolman disease.]. 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:10627498;
prov:wasDerivedFrom dgn-void:befree-2016;
prov:wasGeneratedBy bfo:ECO_0000203 .
dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
dgn-void:source_evidence_literature a bfo:ECO_0000212;
rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP271930.RAuBp4p-ZiGn-ONIsf0W_8gsnd8VgGMIW2u3tTtXw4jRg130_publicationInfo {
this: dcterms:created "2016-05-13T12:43:49+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" .
}