@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI
> .
@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:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_head
{
this:
np:hasAssertion
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_assertion
;
np:hasProvenance
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_provenance
;
np:hasPublicationInfo
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_assertion
a
np:Assertion
.
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_provenance
a
np:Provenance
.
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0029445
a
ncit:C7057
.
dgn-gda:DGNdeb44c6856c8c0b98bc6c6e9099de2c4
sio:SIO_000628
miriam-gene:4524
,
lld:C0029445
;
a
sio:SIO_001122
.
}
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_provenance
{
dgn-np:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_assertion
dcterms:description
"[ Genotypes of PAI-1 4G/5G and MTHFR C677T or plasma concentrations of PAI-1 Ag and tHcy had no effect on the incidence of ONFH in Japanese subjects, unlike the results of studies performed in white subjects. The effect of genetic background on the pathologic conditions that developed in patients with postrenal transplant ONFH may differ according to race.]. 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:14742985
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP61436.RAUiEwnrtlxoKa4Vi9z-N-nxXfTw9T5RSyKZtI5aRR0xI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}