@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY
> .
@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:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_head
{
this:
np:hasAssertion
dgn-np:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_assertion
;
np:hasProvenance
dgn-np:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_provenance
;
np:hasPublicationInfo
dgn-np:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_assertion
a
np:Assertion
.
dgn-np:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_provenance
a
np:Provenance
.
dgn-np:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_assertion
{
miriam-gene:8504
a
ncit:C16612
.
lld:C0020305
a
ncit:C7057
.
dgn-gda:DGN0cec3b992ec01e3a604d4c58b6926224
sio:SIO_000628
miriam-gene:8504
,
lld:C0020305
;
a
sio:SIO_001121
.
}
dgn-np:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_provenance
{
dgn-np:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_assertion
dcterms:description
"[This case also raises a possibility that hydrops fetalis may be associated with a PEX3 gene defect and that peroxisomal disorders can be considered in the etiology of hydrops fetalis as well as other cell organelle disorders when one is considering yet undiscovered complementation groups in peroxisomal disorders.]. 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:20033294
;
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:NP873923.RAr6FwId_RcUwaiK_iravfpvZrvHjtxnXLwx6D7dUVbKY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}