@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY
> .
@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:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_head
{
this:
np:hasAssertion
dgn-np:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_assertion
;
np:hasProvenance
dgn-np:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_provenance
;
np:hasPublicationInfo
dgn-np:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_assertion
a
np:Assertion
.
dgn-np:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_provenance
a
np:Provenance
.
dgn-np:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0000786
a
ncit:C7057
.
dgn-gda:DGN076a184858782b8b897d7ff6d59ddb2c
sio:SIO_000628
miriam-gene:4524
,
lld:C0000786
;
a
sio:SIO_001121
.
}
dgn-np:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_provenance
{
dgn-np:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_assertion
dcterms:description
"[The frequency of the MTHFR gene T allele, which has been reported to be associated with miscarriages, in patients suffering fetal loss was rather significantly lower than in controls whereas there was no difference in the frequency of the eNOS gene A allele.]. 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:15214944
;
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:NP286020.RADAEmyvfTOGJUiGkXPal5xfXj9UnXBsm6lta-bilb-vY130_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" .
}