@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww
> .
@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:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_head
{
this:
np:hasAssertion
dgn-np:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_assertion
;
np:hasProvenance
dgn-np:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_provenance
;
np:hasPublicationInfo
dgn-np:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_assertion
a
np:Assertion
.
dgn-np:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_provenance
a
np:Provenance
.
dgn-np:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_assertion
{
miriam-gene:54514
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGN0c5ba5e60be10c5659bea1825de795f0
sio:SIO_000628
miriam-gene:54514
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_provenance
{
dgn-np:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_assertion
dcterms:description
"[The expression of VASA mRNA and protein was significantly decreased in the sperm of oligozoospermic men, which suggested the lower expression of the VASA gene might be associated with pathogenesis in some subtypes of male infertility and VASA could be used as a molecular marker for the diagnosis of male infertility.]. 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:17486274
;
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:NP674885.RAsdVLvn5KfieUghA3srrffgbhITk_qJt7k2-fry9M_Ww130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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" .
}