@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M
> .
@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:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_head
{
this:
np:hasAssertion
dgn-np:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_assertion
;
np:hasProvenance
dgn-np:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_provenance
;
np:hasPublicationInfo
dgn-np:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_assertion
a
np:Assertion
.
dgn-np:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_provenance
a
np:Provenance
.
dgn-np:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_assertion
{
miriam-gene:3973
a
ncit:C16612
.
lld:C0041408
a
ncit:C7057
.
dgn-gda:DGN3273800539a377ba3f3a439c52609c9c
sio:SIO_000628
miriam-gene:3973
,
lld:C0041408
;
a
sio:SIO_001121
.
}
dgn-np:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_provenance
{
dgn-np:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_assertion
dcterms:description
"[The aim of our study was to specify the respective impact of the interindividual varying status of mosaicism and of hypergonadotropic hypogonadism as well as of the risk factors recurrent OM and HI in comparison to familial coinfluences on the neuromotor proficiency (MOP) in TS.]. 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:12486504
;
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:NP560148.RAZRoIKkPs33htJjkwJUa_qGNr8U7hVLZkDcefo6Ptv_M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}