@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg
> .
@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:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_head
{
this:
np:hasAssertion
dgn-np:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_assertion
;
np:hasProvenance
dgn-np:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_provenance
;
np:hasPublicationInfo
dgn-np:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_assertion
a
np:Assertion
.
dgn-np:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_provenance
a
np:Provenance
.
dgn-np:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_assertion
{
miriam-gene:1617
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGN31e2468f6635f2c221a22351f06e6bea
sio:SIO_000628
miriam-gene:1617
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_provenance
{
dgn-np:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_assertion
dcterms:description
"[The presence of deletions that do not overlap with the DAZ region suggests that genes other than the DAZ gene may also be implicated in the pathogenesis of some subsets of male infertility.]. 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:8636331
;
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:NP650338.RALi78D9v14vtMDLgDIe7btQz0LsT8Jn8yQspHMNgnYOg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:32+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" .
}