@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_head
{
this:
np:hasAssertion
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_assertion
;
np:hasProvenance
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_assertion
a
np:Assertion
.
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_provenance
a
np:Provenance
.
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_assertion
{
miriam-gene:9360
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN13d4c3ff09d012fe4875d13b7f2d5bb6
sio:SIO_000628
miriam-gene:9360
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_provenance
{
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_assertion
dcterms:description
"[Among other genetic markers, thrombophilic genetic variants, such as the Factor V Leiden and prothrombin G20210A polymorphisms, as well as genetic variants of cytochrome P450 (CYP) enzymes, for example, CYP19 and CYP1B1, have been established as genetic risk markers and disease modifiers of recurrent and sporadic pregnancy loss and HRT-independent and -dependent breast cancer, respectively.]. 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:14683420
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:57+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}