@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50
> .
@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:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_head
{
this:
np:hasAssertion
dgn-np:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_assertion
;
np:hasProvenance
dgn-np:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_provenance
;
np:hasPublicationInfo
dgn-np:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_assertion
a
np:Assertion
.
dgn-np:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_provenance
a
np:Provenance
.
dgn-np:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_assertion
{
miriam-gene:283120
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN7391a2e3698af962bc2cbec2419ca208
sio:SIO_000628
miriam-gene:283120
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_provenance
{
dgn-np:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_assertion
dcterms:description
"[We demonstrate correct genetic imprints for H19 even in spermatogonia selected from seminiferous tubules exhibiting spermatogenic arrest at the level of spermatogonia, providing no evidence for incorrect genomic imprinting in spermatozoa from infertile men used for ICSI.]. 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:16608903
;
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:NP470754.RAu-WIPp5s6DnSB6-LRtRn-IdDctLloHYY1w8O5je5A50130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}