@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ
> .
@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:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_head
{
this:
np:hasAssertion
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_assertion
;
np:hasProvenance
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_assertion
a
np:Assertion
.
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_provenance
a
np:Provenance
.
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_assertion
{
miriam-gene:412
a
ncit:C16612
.
lld:C0020619
a
ncit:C7057
.
dgn-gda:DGNdcfc32bb414365836dd3af9eaed0500c
sio:SIO_000628
miriam-gene:412
,
lld:C0020619
;
a
sio:SIO_001121
.
}
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_provenance
{
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_assertion
dcterms:description
"[Flow cytometry and the use of special probes indicated that these two brothers had a large deletion of the short arm of the X chromosome which included the STS locus, the closely linked locus DXS237 and probably the gene for hypogonadism, findings which offer the opportunity for speculations on the locus of control of normal testicular development and function.]. 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:3150366
;
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:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:31+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" .
}