@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs
> .
@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:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_head
{
this:
np:hasAssertion
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_assertion
;
np:hasProvenance
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_provenance
;
np:hasPublicationInfo
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_assertion
a
np:Assertion
.
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_provenance
a
np:Provenance
.
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_assertion
{
miriam-gene:5498
a
ncit:C16612
.
lld:C0162531
a
ncit:C7057
.
dgn-gda:DGNc35f6c069d2d46d29250ab686d6771b0
sio:SIO_000628
miriam-gene:5498
,
lld:C0162531
;
a
sio:SIO_001121
.
}
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_provenance
{
dgn-np:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_assertion
dcterms:description
"[There are seven main types of porphyrias; acute intermittent porphyria and plumboporphyria are predominantly neuropsychiatric; congenital erythropoietic porphyria, porphyria cutanea tarda and erythropoietic protoporphyria have predominantly cutaneous manifestations and hereditary coproporphyria and variegate porphyria are classified as mixed as they both have neuropsychiatric and cutaneous features.]. 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:18541093
;
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:NP393980.RARLeQ7hf_kRaN_jRkBOTsQd7aCGd-1f0MHs8PsXtRycs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}