@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI
> .
@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:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_head
{
this:
np:hasAssertion
dgn-np:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_assertion
;
np:hasProvenance
dgn-np:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_provenance
;
np:hasPublicationInfo
dgn-np:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_assertion
a
np:Assertion
.
dgn-np:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_provenance
a
np:Provenance
.
dgn-np:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C0162566
a
ncit:C7057
.
dgn-gda:DGN00e674d909f71db99f3178618b5c89b9
sio:SIO_000628
miriam-gene:7389
,
lld:C0162566
;
a
sio:SIO_001121
.
}
dgn-np:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_provenance
{
dgn-np:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_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:NP1308054.RAhagh7eqG488BekWrNWisIYL-wHXJYDtSc8MMv1_X7QI130_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" .
}