@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0
> .
@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:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_head
{
this:
np:hasAssertion
dgn-np:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_assertion
;
np:hasProvenance
dgn-np:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_provenance
;
np:hasPublicationInfo
dgn-np:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_assertion
a
np:Assertion
.
dgn-np:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_provenance
a
np:Provenance
.
dgn-np:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNddfae4d2c2ad559e19e0f3333beed375
sio:SIO_000628
miriam-gene:1312
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_provenance
{
dgn-np:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_assertion
dcterms:description
"[This case control study investigated whether polymorphisms of estrogen metabolizing genes CYP1A1 MspI, CYP17 MspAI, COMT Val(158) Met, and SULT1A1 Arg(213) His have any role in familial breast cancer susceptibility risk.]. 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:19863350
;
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:NP59906.RATjWpO6rpDSoRCHo6_ZB3RKotnH86vGJLGFD_2zKpFk0130_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" .
}