@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U
> .
@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:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_head
{
this:
np:hasAssertion
dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_assertion
;
np:hasProvenance
dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_provenance
;
np:hasPublicationInfo
dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_assertion
a
np:Assertion
.
dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_provenance
a
np:Provenance
.
dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0741237
a
ncit:C7057
.
dgn-gda:DGN284993821cb405cb22c85f82797c1ce2
sio:SIO_000628
miriam-gene:3077
,
lld:C0741237
;
a
sio:SIO_001121
.
}
dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_provenance
{
dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_assertion
dcterms:description
"[More detailed study of arthritis symptoms and signs over time in individuals with and without mutations in the HFE gene is necessary to determine the contribution of HFE genes to arthritis in the population.]. 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:14673391
;
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:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}