@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU
> .
@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:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_head
{
this:
np:hasAssertion
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_assertion
;
np:hasProvenance
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_provenance
;
np:hasPublicationInfo
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_assertion
a
np:Assertion
.
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_provenance
a
np:Provenance
.
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_assertion
{
miriam-gene:4313
a
ncit:C16612
.
lld:C0033860
a
ncit:C7057
.
dgn-gda:DGN9c33e0234c54f171aeaaa5984310f291
sio:SIO_000628
miriam-gene:4313
,
lld:C0033860
;
a
sio:SIO_001121
.
}
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_provenance
{
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_assertion
dcterms:description
"[Although no significant case-control differences in frequency of associated GG(-1575)CC(-1306)TT(-790) MMP-2 promoter genotype were observed, the genotype was found to be significantly less frequent in patients with family history of psoriasis (close as well as distant), family history of diabetes and personal history of allergy (2/11 vs. 55/32, odds ratio (OR) for GGCCTT 0.11, 95% confidential interval 0.02-0.50, Pcorr = 0.01).]. 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:19360430
;
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:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:29+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" .
}