@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4
> .
@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:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_head
{
this:
np:hasAssertion
dgn-np:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_assertion
;
np:hasProvenance
dgn-np:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_provenance
;
np:hasPublicationInfo
dgn-np:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_assertion
a
np:Assertion
.
dgn-np:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_provenance
a
np:Provenance
.
dgn-np:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_assertion
{
miriam-gene:3973
a
ncit:C16612
.
lld:C0022735
a
ncit:C7057
.
dgn-gda:DGN75297b1962cd3789485b361e30c63002
sio:SIO_000628
miriam-gene:3973
,
lld:C0022735
;
a
sio:SIO_001121
.
}
dgn-np:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_provenance
{
dgn-np:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_assertion
dcterms:description
"[Although the more complex chromosome aneuploidies 48, XXYY, 48, XXXY, and 49, XXXXY are often compared with 47, XXY (Klinefelter syndrome) because of shared features including tall stature and hypergonadotropic hypogonadism, there is a wider spectrum of physical and cognitive abilities that have recently been delineated.]. 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:23335129
;
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:NP417172.RA9HxeKkDFdJF4_yQh-7q-ANgU08f0FeXhAF-b_liCk_4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:07+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" .
}