@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA
> .
@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:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_head
{
this:
np:hasAssertion
dgn-np:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_assertion
;
np:hasProvenance
dgn-np:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_provenance
;
np:hasPublicationInfo
dgn-np:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_assertion
a
np:Assertion
.
dgn-np:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_provenance
a
np:Provenance
.
dgn-np:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_assertion
{
miriam-gene:253175
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGNde9d9c9ae7d040ab40d1f107a4f08d26
sio:SIO_000628
miriam-gene:253175
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_provenance
{
dgn-np:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_assertion
dcterms:description
"[Therefore, there was no clear relation between genotype and phenotype, and the loss of the distal copy of CDY1 does not seem to worsen the phenotype of infertile patients with deletion of the DAZ gene cluster.]. 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:11263480
;
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:NP480412.RAraW8727Q_S4x89YMst-hqLjRvvYRbgSFCGpU5h_xlkA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:47+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" .
}