@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4
> .
@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:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_head
{
this:
np:hasAssertion
dgn-np:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_assertion
;
np:hasProvenance
dgn-np:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_provenance
;
np:hasPublicationInfo
dgn-np:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_assertion
a
np:Assertion
.
dgn-np:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_provenance
a
np:Provenance
.
dgn-np:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN29bbc826de32f270979e8b94998f0c5f
sio:SIO_000628
miriam-gene:1543
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_provenance
{
dgn-np:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_assertion
dcterms:description
"[The increased risk of breast cancer associated with E+P use was greater among women with at least one rare allele of the CYP1A1 Ile(462)Val, CYP1A1 MspI, CYP1B1 Asn(453)Ser, and PGR Val(660)Leu polymorphisms than among women homozygous for the common allele of these polymorphisms.]. 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:18628428
;
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:NP182772.RASmjDoZY27wCjIfnI9CweFlqHzFtVAM226WTaTQmaee4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}