@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY
> .
@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:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_head
{
this:
np:hasAssertion
dgn-np:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_assertion
;
np:hasProvenance
dgn-np:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_provenance
;
np:hasPublicationInfo
dgn-np:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_assertion
a
np:Assertion
.
dgn-np:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_provenance
a
np:Provenance
.
dgn-np:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_assertion
{
miriam-gene:128674
a
ncit:C16612
.
lld:C0022735
a
ncit:C7057
.
dgn-gda:DGNec8560c239abc531dd22c2eec839e6f1
sio:SIO_000628
miriam-gene:128674
,
lld:C0022735
;
a
sio:SIO_001121
.
}
dgn-np:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_provenance
{
dgn-np:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_assertion
dcterms:description
"[Our goal was to determine whether variants in the first intracellular loop (ICL1) of PROKR2 (R80C, R85C, and R85H) identified in patients with hypogonadotropic hypogonadism interfere with receptor function and to elucidate the mechanisms of these effects.]. 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:22745195
;
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:NP611275.RA8JTmFY-1NqSkB0HKRcX9zEUmbEeDJAwTcFRaj3O_4iY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:09+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" .
}