@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w
> .
@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:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_head
{
this:
np:hasAssertion
dgn-np:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_assertion
;
np:hasProvenance
dgn-np:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_provenance
;
np:hasPublicationInfo
dgn-np:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_assertion
a
np:Assertion
.
dgn-np:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_provenance
a
np:Provenance
.
dgn-np:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNd8ce8824ed7267037f71500f699edc80
sio:SIO_000628
miriam-gene:1312
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_provenance
{
dgn-np:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_assertion
dcterms:description
"[Pairwise analysis showed that combinations of the ERalpha G allele with the homozygous Trp genotype of CYP19A1 codon 39 (rs2236722), the methionine (Met) allele of COMT codon 158 (rs4680) or Pro allele of p53 codon 72 (rs1042522) were more frequent in ER-positive than ER-negative breast cancer, especially in patients less than 50-year old.]. 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:18820009
;
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:NP59907.RAQFKngdFgsi1XQHz01xgCt8lL85n6iq_NJgk9-ILJc4w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}