@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg
> .
@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:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_head
{
this:
np:hasAssertion
dgn-np:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_assertion
;
np:hasProvenance
dgn-np:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_provenance
;
np:hasPublicationInfo
dgn-np:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_assertion
a
np:Assertion
.
dgn-np:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_provenance
a
np:Provenance
.
dgn-np:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_assertion
{
miriam-gene:2263
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN394fce9392797879c3574ed891eddabe
sio:SIO_000628
miriam-gene:2263
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_provenance
{
dgn-np:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_assertion
dcterms:description
"[A recent genome-wide association study has shown that common alleles at single nucleotide polymorphisms (SNPs) in FGFR2 (rs2981582), TNRC9 (rs3803662), and MAP3K1 (rs889312) are associated with increased breast cancer risks in the general population.]. 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:18355772
;
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:NP250078.RA7HOJYkPRl9PDZuXLN8y407GWcF82NBGyy_bcc9PCgfg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}