@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k
> .
@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:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_head
{
this:
np:hasAssertion
dgn-np:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_assertion
;
np:hasProvenance
dgn-np:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_provenance
;
np:hasPublicationInfo
dgn-np:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_assertion
a
np:Assertion
.
dgn-np:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_provenance
a
np:Provenance
.
dgn-np:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_assertion
{
miriam-gene:560
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN109cf2a1e1a4e0ee21e071e10cd8880e
sio:SIO_000628
miriam-gene:560
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_provenance
{
dgn-np:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_assertion
dcterms:description
"[Therefore, testing for Y chromosome microdeletions should be considered as an important element in diagnosis and genetic counseling of infertile men in Serbia and decisions regarding the assisted reproduction should be made based on the presence and type of AZF microdeletions.]. 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:17853812
;
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:NP162283.RA8_67ITlie-stxYQeSm2mcH-9go2nRb2iWMcqtLsLr4k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}