@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg
> .
@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:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_head
{
this:
np:hasAssertion
dgn-np:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_assertion
;
np:hasProvenance
dgn-np:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_provenance
;
np:hasPublicationInfo
dgn-np:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_assertion
a
np:Assertion
.
dgn-np:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_provenance
a
np:Provenance
.
dgn-np:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0011644
a
ncit:C7057
.
dgn-gda:DGN5aa59505772a12b1416875e68fba7cd1
sio:SIO_000628
miriam-gene:3133
,
lld:C0011644
;
a
sio:SIO_001121
.
}
dgn-np:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_provenance
{
dgn-np:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_assertion
dcterms:description
"[The purpose of this study was to investigate tumor necrosis factor (TNF) polymorphisms in scleroderma, with the specific aim of determining whether TNF polymorphisms would prove to be stronger markers for ACA than class II major histocompatibility complex (MHC).]. 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:14872499
;
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:NP922322.RAmWcCv3-AAU7UDK02hpVNAVMEL3kN__JjfjspEN20Cyg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:26+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" .
}