@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_head
{
this:
np:hasAssertion
dgn-np:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_assertion
;
np:hasProvenance
dgn-np:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_provenance
;
np:hasPublicationInfo
dgn-np:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_assertion
a
np:Assertion
.
dgn-np:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_provenance
a
np:Provenance
.
dgn-np:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C0268323
a
ncit:C7057
.
dgn-gda:DGN28fce89179c6d64045f5dd6712f55815
sio:SIO_000628
miriam-gene:7389
,
lld:C0268323
;
a
sio:SIO_001121
.
}
dgn-np:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_provenance
{
dgn-np:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_assertion
dcterms:description
"[Inheritance of an autosomal dominant gene which decreases uroporphyrinogen decarboxylase activity in erythrocytes and liver is an uncommon cause of porphyria cutanea tarda and may not explain all cases of familial porphyria cutanea tarda.]. 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:7428280
;
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:NP1308053.RANNtDfaQSk2CAtMpXa3J3WOba6v2I6QfOM4HYn5Puixc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:39+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}