@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs
> .
@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:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_head
{
this:
np:hasAssertion
dgn-np:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_assertion
;
np:hasProvenance
dgn-np:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_provenance
;
np:hasPublicationInfo
dgn-np:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_assertion
a
np:Assertion
.
dgn-np:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_provenance
a
np:Provenance
.
dgn-np:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_assertion
{
miriam-gene:54808
a
ncit:C16612
.
lld:C0041408
a
ncit:C7057
.
dgn-gda:DGNf0946b18a442b1d981096b3733d1e5a2
sio:SIO_000628
miriam-gene:54808
,
lld:C0041408
;
a
sio:SIO_001121
.
}
dgn-np:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_provenance
{
dgn-np:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_assertion
dcterms:description
"[DNA and FISH (fluorescence in situ hybridization) analysis were carried out in 12 patients with stigmata of Turner syndrome to determine whether the Supernumerary Marker Chromosome (SMC) found cytogenetically in each of these patients was derived from the Y chromosome.]. 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:9137884
;
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:NP299936.RAYurgQH8fnUR1ntFzr0sdiqVO8rLzP4Qmk_14tX1zWSs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}