@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk
> .
@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:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_head
{
this:
np:hasAssertion
dgn-np:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_assertion
;
np:hasProvenance
dgn-np:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_provenance
;
np:hasPublicationInfo
dgn-np:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_assertion
a
np:Assertion
.
dgn-np:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_provenance
a
np:Provenance
.
dgn-np:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_assertion
{
miriam-gene:2235
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGNfe6651bda2ed23c870824f66a10b2bd6
sio:SIO_000628
miriam-gene:2235
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_provenance
{
dgn-np:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_assertion
dcterms:description
"[The cDNA for human ferrochelatase, the enzyme that is defective in the rare genetic disease erythropoietic protoporphyria (EPP), was tested for its ability to allow the expression of ferrochelatase in mammalian cells.]. 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:7706765
;
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:NP167786.RAsZlqBasQJYJ17xC3wQ8VpsnIfcQE8Dss4TGGM-QvdWk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}