@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY
> .
@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:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_head
{
this:
np:hasAssertion
dgn-np:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_assertion
;
np:hasProvenance
dgn-np:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_provenance
;
np:hasPublicationInfo
dgn-np:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_assertion
a
np:Assertion
.
dgn-np:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_provenance
a
np:Provenance
.
dgn-np:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0282193
a
ncit:C7057
.
dgn-gda:DGN144ebc6690fd67c9a5615954971f51b2
sio:SIO_000628
miriam-gene:7124
,
lld:C0282193
;
a
sio:SIO_001121
.
}
dgn-np:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_provenance
{
dgn-np:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_assertion
dcterms:description
"[In patients with homozygous C282Y hemochromatosis, we investigated the influence of TNF-alpha -308G>A allelic variant on total body iron overload, determined in all patients by measuring iron removed during depletion therapy, and hepatic iron index and need for phlebotomy to prevent iron reaccumulation, measured in patient subgroups.]. 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:16793930
;
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:NP319232.RAjfF3yNDYwVv8X2MQ70y5FCwXUbQFPu_b5xUGG7-4rbY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:05+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" .
}