@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g
> .
@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:NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g130_head
{
this:
np:hasAssertion
dgn-np:NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g130_assertion
;
np:hasProvenance
dgn-np:NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g130_provenance
;
np:hasPublicationInfo
dgn-np:NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g130_publicationInfo
;
a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g130_provenance
a
np:Provenance
.
dgn-np:NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g130_assertion
{
miriam-gene:159119
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGNc47ff75243b5517361aed04cbb5a3d99
sio:SIO_000628
miriam-gene:159119
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g130_provenance
{
dgn-np:NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g130_assertion
dcterms:description
"[We screened 1186 men from infertile couples for Y chromosome deletions, and identified three unrelated oligozoospermic men and one azoospermic man who carry an identical 768 kb deletion resulting in loss of the entire P4 palindrome, including both HSFY genes, the only coding genes within the deletion interval.]. 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:22158087
;
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:NP259240.RA-ZChChFQSfmtLgcNRbr9UWFUTD6mu29AJD85006CT_g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:24+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
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prv:usedData
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<
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> , <
http://orcid.org/0000-0002-7534-7661
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> , <
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
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"v2.1.0" .
}