@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM
> .
@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:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_head
{
this:
np:hasAssertion
dgn-np:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_assertion
;
np:hasProvenance
dgn-np:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_provenance
;
np:hasPublicationInfo
dgn-np:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_assertion
a
np:Assertion
.
dgn-np:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_provenance
a
np:Provenance
.
dgn-np:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_assertion
{
miriam-gene:7077
a
ncit:C16612
.
lld:C0278996
a
ncit:C7057
.
dgn-gda:DGN0a5548db2cb0e8e87dab76dd2d5f68b6
sio:SIO_000628
miriam-gene:7077
,
lld:C0278996
;
a
sio:SIO_001121
.
}
dgn-np:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_provenance
{
dgn-np:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_assertion
dcterms:description
"[Furthermore, the polymorphisms in both genes showed some additive effect and the highest risk for head and neck cancer was observed in those with MMP2 CC genotype and TIMP2 variant GC or CC genotype (OR, 2.34; 95% CI, 1.31-4.18).]. 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:16275157
;
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:NP848173.RAVrQzeSOCSv03pbfcFjRfBiOKP1OgoxpYhz1cSS_TNlM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:38+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" .
}