@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA
> .
@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:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_head
{
this:
np:hasAssertion
dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_assertion
;
np:hasProvenance
dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_provenance
;
np:hasPublicationInfo
dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_assertion
a
np:Assertion
.
dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_provenance
a
np:Provenance
.
dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN972b9f40238f2926f1d7c7d41904266a
sio:SIO_000628
miriam-gene:2153
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_provenance
{
dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_assertion
dcterms:description
"[Factor V Leiden (FVL) G1691A, methylenetetrahydrofolate reductase (MTHFR) C677T, and factor II (FII) G20210A mutations are three important causes of thrombophilia, the condition that might be related to infertility and recurrent spontaneous abortion (RSA).]. 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:16450127
;
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:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:30+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" .
}