@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w
> .
@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:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_head
{
this:
np:hasAssertion
dgn-np:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_assertion
;
np:hasProvenance
dgn-np:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_provenance
;
np:hasPublicationInfo
dgn-np:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_assertion
a
np:Assertion
.
dgn-np:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_provenance
a
np:Provenance
.
dgn-np:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_assertion
{
miriam-gene:2162
a
ncit:C16612
.
lld:C0040053
a
ncit:C7057
.
dgn-gda:DGN3ec48dfde3b64577b0833c13f4000b77
sio:SIO_000628
miriam-gene:2162
,
lld:C0040053
;
a
sio:SIO_001122
.
}
dgn-np:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_provenance
{
dgn-np:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_assertion
dcterms:description
"[Some differences were observed among cases and controls in the prevalence of 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:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP134437.RAEjiuZJSUjPiwx6hXMfMGzawUr71lOUYwXtiCwLmty4w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:10+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" .
}