@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP84113.RADtmp3wv7KH01tPhiU8I-wz0_BE9LW5UZXDtOb26fzwA
> .
@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:NP84113.RADtmp3wv7KH01tPhiU8I-wz0_BE9LW5UZXDtOb26fzwA130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP84113.RADtmp3wv7KH01tPhiU8I-wz0_BE9LW5UZXDtOb26fzwA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP84113.RADtmp3wv7KH01tPhiU8I-wz0_BE9LW5UZXDtOb26fzwA130_assertion
a
np:Assertion
.
dgn-np:NP84113.RADtmp3wv7KH01tPhiU8I-wz0_BE9LW5UZXDtOb26fzwA130_provenance
a
np:Provenance
.
dgn-np:NP84113.RADtmp3wv7KH01tPhiU8I-wz0_BE9LW5UZXDtOb26fzwA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP84113.RADtmp3wv7KH01tPhiU8I-wz0_BE9LW5UZXDtOb26fzwA130_assertion
{
miriam-gene:4313
a
ncit:C16612
.
lld:C0026654
a
ncit:C7057
.
dgn-gda:DGN314fa77fa54c0273750d1421718656e1
sio:SIO_000628
miriam-gene:4313
,
lld:C0026654
;
a
sio:SIO_001122
.
}
dgn-np:NP84113.RADtmp3wv7KH01tPhiU8I-wz0_BE9LW5UZXDtOb26fzwA130_provenance
{
dgn-np:NP84113.RADtmp3wv7KH01tPhiU8I-wz0_BE9LW5UZXDtOb26fzwA130_assertion
dcterms:description
"[The functional polymorphism in the MMP-3 promoter might be associated with susceptibility to both MMD and FMMD in the Chinese Han population. The findings need to be validated in further studies including more subjects from different populations.]. 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:20948207
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP84113.RADtmp3wv7KH01tPhiU8I-wz0_BE9LW5UZXDtOb26fzwA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:41+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
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pav:authoredBy
<
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
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"v2.1.0" .
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