@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY
> .
@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:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_head
{
this:
np:hasAssertion
dgn-np:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_assertion
;
np:hasProvenance
dgn-np:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_provenance
;
np:hasPublicationInfo
dgn-np:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_assertion
a
np:Assertion
.
dgn-np:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_provenance
a
np:Provenance
.
dgn-np:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_assertion
{
miriam-gene:10911
a
ncit:C16612
.
lld:C0333068
a
ncit:C7057
.
dgn-gda:DGN64867a1f1860ea41bb915da6b3696ca5
sio:SIO_000628
miriam-gene:10911
,
lld:C0333068
;
a
sio:SIO_001121
.
}
dgn-np:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_provenance
{
dgn-np:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_assertion
dcterms:description
"[There were significant associations between the genotype and allele frequencies of UTS2 gene Thr21Met polymorphism and cases with diffuse or limited SSc, systemic or lung involvement, finger flexion deformity, pitting scars at the fingertips, positive anticentromere, or positive antitopoisomerase 1 antibody groups.]. 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:22045841
;
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:NP356334.RAd2ewKFGjp4YGW3sLIxeREzI5D5ulMumMNmyhFF0YrUY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:29+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" .
}