@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow
> .
@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:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_head
{
this:
np:hasAssertion
dgn-np:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_assertion
;
np:hasProvenance
dgn-np:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_provenance
;
np:hasPublicationInfo
dgn-np:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_assertion
a
np:Assertion
.
dgn-np:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_provenance
a
np:Provenance
.
dgn-np:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_assertion
{
miriam-gene:181
a
ncit:C16612
.
lld:C0004509
a
ncit:C7057
.
dgn-gda:DGN2c21789398a419aaa8039674f86acdd7
sio:SIO_000628
miriam-gene:181
,
lld:C0004509
;
a
sio:SIO_001121
.
}
dgn-np:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_provenance
{
dgn-np:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_assertion
dcterms:description
"[To review established genetic causes of azoospermia, the most severe form of male infertility, and help clinicians, scientists, and infertile couples considering assisted reproductive technologies (ART) to understand the complexity of the disorder and to maximize the chances of having a healthy infant through proper counseling and treatment.]. 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:21195467
;
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:NP559722.RAqLCJJux8AW2bBwC7HEaNPsgQTBj9os7NBWrw8I_iUow130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:37+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" .
}