@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM
> .
@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:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_head
{
this:
np:hasAssertion
dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_assertion
;
np:hasProvenance
dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_provenance
;
np:hasPublicationInfo
dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_assertion
a
np:Assertion
.
dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_provenance
a
np:Provenance
.
dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_assertion
{
miriam-gene:5053
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNe0cdbddaf93c815f53768144daa36868
sio:SIO_000628
miriam-gene:5053
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_provenance
{
dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_assertion
dcterms:description
"[Nevertheless, there is fair agreement that a variety of factors may increase risk for SAB or RAB, including advanced maternal age, single gene mutations such as PKU or G6PD deficiency, structural abnormalities of the uterus, poorly controlled diabetes, antiphospholipid syndrome, and smoking.]. 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:11355791
;
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:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}