@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI
> .
@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:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_head
{
this:
np:hasAssertion
dgn-np:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_assertion
;
np:hasProvenance
dgn-np:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_provenance
;
np:hasPublicationInfo
dgn-np:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_assertion
a
np:Assertion
.
dgn-np:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_provenance
a
np:Provenance
.
dgn-np:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGNc0bec09263223f29a7175c29aec599cd
sio:SIO_000628
miriam-gene:5660
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_provenance
{
dgn-np:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_assertion
dcterms:description
"[PSAP is a neurotrophic molecule; its deficiency or inactivation has proved to be lethal in man and mice, and in mice, it leads to abnormal development and atrophy of the prostate gland, despite normal testosterone levels.]. 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:16080200
;
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:NP492716.RAcGQhBrdcs7dXBE1e_UaHmpt6QO9Cm66OMEsLCmqsonI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:54+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" .
}