@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo
> .
@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:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_head
{
this:
np:hasAssertion
dgn-np:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_assertion
;
np:hasProvenance
dgn-np:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_provenance
;
np:hasPublicationInfo
dgn-np:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_assertion
a
np:Assertion
.
dgn-np:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_provenance
a
np:Provenance
.
dgn-np:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_assertion
{
miriam-gene:7390
a
ncit:C16612
.
lld:C0162565
a
ncit:C7057
.
dgn-gda:DGNd545b7d9ad65083a1f0cbee058fe16f9
sio:SIO_000628
miriam-gene:7390
,
lld:C0162565
;
a
sio:SIO_001121
.
}
dgn-np:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_provenance
{
dgn-np:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_assertion
dcterms:description
"[1. delta-Aminolevulinic acid dehydratase (ALA-D), blood lead and several enzymes and metabolites of the heme biosynthetic pathway were measured in a number of symptomatic porphyric patients, 22 with acute intermittent porphyria, three with hereditary hepatic coproporphyria, 10 with hereditary porphyria cutanea tarda, two with erythropoietic protoporphyria and two with congenital erythropoietic porphyria and in 84 lead intoxicated persons.]. 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:3622905
;
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:NP720822.RAaYAWv41C7NWXhcoGmDSp3EPI0Z__6iIQ72EsOKsOOQo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}