@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_head
{
this:
np:hasAssertion
dgn-np:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_assertion
;
np:hasProvenance
dgn-np:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_provenance
;
np:hasPublicationInfo
dgn-np:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_assertion
a
np:Assertion
.
dgn-np:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_provenance
a
np:Provenance
.
dgn-np:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C0037061
a
ncit:C7057
.
dgn-gda:DGN0e5d543e9c355e9685e1cd0d257c5642
sio:SIO_000628
miriam-gene:7389
,
lld:C0037061
;
a
sio:SIO_001121
.
}
dgn-np:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_provenance
{
dgn-np:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_assertion
dcterms:description
"[Subnormal activity of hepatic uroporphyrinogen decarboxylase is responsible for the derangement of porphyrin biosynthesis in both sporadic and familial porphyria cutanea tarda, but the enzymatic defect is not clinically expressed in the absence of hepatic siderosis.]. 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:3979748
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP506602.RAPqWD9s7jQmPTZfs1KVJGzjPWb5g8z70-xOAjutVkL-o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:02+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}