@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_head
{
this:
np:hasAssertion
dgn-np:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_assertion
;
np:hasProvenance
dgn-np:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_provenance
;
np:hasPublicationInfo
dgn-np:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_assertion
a
np:Assertion
.
dgn-np:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_provenance
a
np:Provenance
.
dgn-np:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0153690
a
ncit:C7057
.
dgn-gda:DGN7def1a0e0c0738e31ac3136e238017a6
sio:SIO_000628
miriam-gene:2099
,
lld:C0153690
;
a
sio:SIO_001122
.
}
dgn-np:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_provenance
{
dgn-np:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_assertion
dcterms:description
"[rs3803662 of TNRC9 gene has been shown to be the SNP with the strongest association with BC, in particular, this polymorphism seems to be correlated with bone metastases and estrogen receptor positivity.]. 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:21996731
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP930812.RAOWa6D0DfC4y41PHoop-k4cfi8XYPQaSwouTi1LVWvR4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:47+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}