@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY
> .
@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:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_head
{
this:
np:hasAssertion
dgn-np:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_assertion
;
np:hasProvenance
dgn-np:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_provenance
;
np:hasPublicationInfo
dgn-np:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_assertion
a
np:Assertion
.
dgn-np:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_provenance
a
np:Provenance
.
dgn-np:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGN940e6c8776df6242d8850bc38de5fa30
sio:SIO_000628
miriam-gene:4524
,
lld:C0009324
;
a
sio:SIO_001122
.
}
dgn-np:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_provenance
{
dgn-np:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_assertion
dcterms:description
"[Although some differences were observed among cases and controls in the prevalence of MTHFR C677T (decrease in mutant allele carriership in UC) and FXIII val34leu (increase in double mutant allele carriership in CD), these did not explain an excess risk of thrombosis.]. 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:17156138
;
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:NP574609.RA1RxI62LlrNeG1BlOA41I9reCD9dRH26CuyA9fKZn3EY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:22+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" .
}