@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc
> .
@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:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_head
{
this:
np:hasAssertion
dgn-np:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_assertion
;
np:hasProvenance
dgn-np:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_provenance
;
np:hasPublicationInfo
dgn-np:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_assertion
a
np:Assertion
.
dgn-np:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_provenance
a
np:Provenance
.
dgn-np:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN9eeb93bf7b52a9a85d78bd9b350c6c68
sio:SIO_000628
miriam-gene:1586
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_provenance
{
dgn-np:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_assertion
dcterms:description
"[In a case-control study of Chinese women, we examined genotypes of the CYP11A1 pentanucleotide [(TAAAA)n] repeat (D15S520), CYP17A1 rs743572, and HSD17B1 rs605059 polymorphisms in relation to the risk of breast cancer and fibrocystic breast conditions, comparing 615 women with breast cancer and 467 women with fibrocystic breast conditions separately with 879 women without clinical breast disease.]. 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:18483327
;
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:NP285605.RAXfwGeU1zv2Rah1u35qGzrcMDpBYIXIKzZo87-5rpSkc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:41+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" .
}