@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870
> .
@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:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_head
{
this:
np:hasAssertion
dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_assertion
;
np:hasProvenance
dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_provenance
;
np:hasPublicationInfo
dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_assertion
a
np:Assertion
.
dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_provenance
a
np:Provenance
.
dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0036421
a
ncit:C7057
.
dgn-gda:DGNa50841d44e457424cc308523fb06a846
sio:SIO_000628
miriam-gene:3133
,
lld:C0036421
;
a
sio:SIO_001121
.
}
dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_provenance
{
dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_assertion
dcterms:description
"[Currently it may be stated that the MHC associations in scleroderma support the classification of disease subsets, but in no ethnic group is the overall association strong enough for clinical use.]. 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:1516246
;
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:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}