@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8
> .
@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:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_head
{
this:
np:hasAssertion
dgn-np:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_assertion
;
np:hasProvenance
dgn-np:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_provenance
;
np:hasPublicationInfo
dgn-np:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_assertion
a
np:Assertion
.
dgn-np:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_provenance
a
np:Provenance
.
dgn-np:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_assertion
{
miriam-gene:3145
a
ncit:C16612
.
lld:C0149676
a
ncit:C7057
.
dgn-gda:DGN1a7bfb55655589f7d89b5cc5613291bf
sio:SIO_000628
miriam-gene:3145
,
lld:C0149676
;
a
sio:SIO_001121
.
}
dgn-np:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_provenance
{
dgn-np:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_assertion
dcterms:description
"[Deficiency of uroporphyrinogen III synthase activity was reflected by inversion of the relationship between and isomer III leading to dominance of isomer I. Elevation of porphobilinogen deaminase activities is related to hemolysis and, additionally, to regulatory compensation for the enzyme deficiency.]. 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:9164637
;
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:NP414022.RAUZ0RGdgmMWcD7DAKAZZJWRKMDTetQzrYQWBDxf1wXq8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:06+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" .
}