@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM
> .
@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:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_head
{
this:
np:hasAssertion
dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_assertion
;
np:hasProvenance
dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_provenance
;
np:hasPublicationInfo
dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_assertion
a
np:Assertion
.
dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_provenance
a
np:Provenance
.
dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_assertion
{
miriam-gene:2235
a
ncit:C16612
.
lld:C0025517
a
ncit:C7057
.
dgn-gda:DGN81a26719b3dbf8a654cf3ab5740685ef
sio:SIO_000628
miriam-gene:2235
,
lld:C0025517
;
a
sio:SIO_001121
.
}
dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_provenance
{
dgn-np:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_assertion
dcterms:description
"[Protoporphyria is an inherited disorder of heme biosynthesis characterized by an overproduction of protoporphyrin in the erythropoietic and hepatic tissues, the relative contribution of which in the metabolic disorder has not been directly quantitated.]. 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:3294082
;
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:NP901564.RA62PfNrMMnmLIzV7HAVpc3YkfOyfmZ8j3BBfMgdgFYvM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:14+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" .
}