@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_head
{
this:
np:hasAssertion
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_assertion
;
np:hasProvenance
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_provenance
;
np:hasPublicationInfo
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_assertion
a
np:Assertion
.
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_provenance
a
np:Provenance
.
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_assertion
{
miriam-gene:100653377
a
ncit:C16612
.
lld:C0028960
a
ncit:C7057
.
dgn-gda:DGNe5decaa31062bdf4c2c22fee63b76d7b
sio:SIO_000628
miriam-gene:100653377
,
lld:C0028960
;
a
sio:SIO_001121
.
}
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_provenance
{
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_assertion
dcterms:description
"[The data indicate that: 1) the composition of the study population is the major factor in determining deletion frequency; 2) Y chromosome microdeletions are specifically associated with severe spermatogenic failure; therefore, the protocol described here is reliable for the routine clinical workup of severe male factor infertility; and 3) the frequency of Yq microdeletions in the Danish population is similar to that from other countries and argues against the involvement of microdeletions in the relatively low sperm count of the Danish population.]. 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:11397865
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:10+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}