@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA
> .
@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 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:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_head
{
this:
np:hasAssertion
dgn-np:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_assertion
;
np:hasProvenance
dgn-np:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_provenance
;
np:hasPublicationInfo
dgn-np:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_assertion
a
np:Assertion
.
dgn-np:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_provenance
a
np:Provenance
.
dgn-np:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_assertion
{
miriam-gene:3673
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN57350931d9d9b6d9e0c482f85c221e56
sio:SIO_000628
miriam-gene:3673
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_provenance
{
dgn-np:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_assertion
dcterms:description
"[We conclude that functional polymorphisms in integrin genes ITGA2 and ITGB3 influence the development and progression of breast cancer, respectively. The precise mechanism remains to be determined, but likely involves dysregulated signaling pathways.]. 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:16317580
;
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:NP55762.RAyKTQqmSqj60BvMafqfCHsL9Ede5F8OXloMGo7DcKZMA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}