@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w
> .
@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:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_head
{
this:
np:hasAssertion
dgn-np:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_assertion
;
np:hasProvenance
dgn-np:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_provenance
;
np:hasPublicationInfo
dgn-np:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_assertion
a
np:Assertion
.
dgn-np:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_provenance
a
np:Provenance
.
dgn-np:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_assertion
{
miriam-gene:5554
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN1431248ccf0c95e911b0e1d94428d691
sio:SIO_000628
miriam-gene:5554
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_provenance
{
dgn-np:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_assertion
dcterms:description
"[Antithrombin and PC deficiencies and the presence of APLA and increased factor VIII levels were more frequent in the pediatric stroke patients than in controls but the difference was not statistically significant (p > 0.05).]. 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:15678277
;
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:NP401369.RAe4kMr4xM6ooaKAotkkgbq41dfYtbyeoc5inqjlpEl2w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}