@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg
> .
@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:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_head
{
this:
np:hasAssertion
dgn-np:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_assertion
;
np:hasProvenance
dgn-np:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_provenance
;
np:hasPublicationInfo
dgn-np:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_assertion
a
np:Assertion
.
dgn-np:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_provenance
a
np:Provenance
.
dgn-np:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_assertion
{
miriam-gene:137902
a
ncit:C16612
.
lld:C0028960
a
ncit:C7057
.
dgn-gda:DGN66545d90376e00b97daca3ea241264aa
sio:SIO_000628
miriam-gene:137902
,
lld:C0028960
;
a
sio:SIO_001121
.
}
dgn-np:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_provenance
{
dgn-np:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_assertion
dcterms:description
"[A total of 160 control individuals and at least 125 infertile men with either idiopathic azoospermia or oligozoospermia were sequenced for the open reading frame of PRM1, PRM2, PRM3 and TNP2 genes.]. 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:19602509
;
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:NP494206.RAMXpHaZjLADCKUXyJ-bKhMPfLfqGyoydhgevIOBd9wRg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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" .
}