@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w
> .
@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:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_head
{
this:
np:hasAssertion
dgn-np:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_assertion
;
np:hasProvenance
dgn-np:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_provenance
;
np:hasPublicationInfo
dgn-np:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_assertion
a
np:Assertion
.
dgn-np:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_provenance
a
np:Provenance
.
dgn-np:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_assertion
{
miriam-gene:4313
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGNc9048396d91718f13550b92ae000ebe7
sio:SIO_000628
miriam-gene:4313
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_provenance
{
dgn-np:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_assertion
dcterms:description
"[In conclusion, MMP2 C735T and C1306T polymorphisms are both associated with lung cancer risk, and patients with high MMP2 expression levels have poorer overall survival compared with those with low MMP2 expression levels.]. 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:22718017
;
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:NP471789.RARqgbdZMbmNYFPG3dkVRLiGtN891Aj6B8Pw_0I7tbd4w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+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" .
}