@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs
> .
@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:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_head
{
this:
np:hasAssertion
dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_assertion
;
np:hasProvenance
dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_provenance
;
np:hasPublicationInfo
dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_assertion
a
np:Assertion
.
dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_provenance
a
np:Provenance
.
dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_assertion
{
miriam-gene:3973
a
ncit:C16612
.
lld:C0851265
a
ncit:C7057
.
dgn-gda:DGN123d661f70eed48ef7b1a7236798cd61
sio:SIO_000628
miriam-gene:3973
,
lld:C0851265
;
a
sio:SIO_001121
.
}
dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_provenance
{
dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_assertion
dcterms:description
"[Chronic manifestations, which also develop in prospectively treated patients, involve (a) the brain, resulting in delayed language acquisition, speech defects, and learning problems, and (b) the ovary, in the majority of females, producing hypergonadotropic hypogonadism.]. 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:18574215
;
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:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:58+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" .
}