@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc
> .
@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:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_head
{
this:
np:hasAssertion
dgn-np:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_assertion
;
np:hasProvenance
dgn-np:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_provenance
;
np:hasPublicationInfo
dgn-np:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_assertion
a
np:Assertion
.
dgn-np:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_provenance
a
np:Provenance
.
dgn-np:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_assertion
{
miriam-gene:6046
a
ncit:C16612
.
lld:C1336708
a
ncit:C7057
.
dgn-gda:DGN8384c8cd59fc99ac9bb468917e5f6845
sio:SIO_000628
miriam-gene:6046
,
lld:C1336708
;
a
sio:SIO_001121
.
}
dgn-np:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_provenance
{
dgn-np:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_assertion
dcterms:description
"[Follicle stimulating hormone (FSH) levels are increased in numerous conditions associated with increased risk of TGCT and single nucleotide polymorphisms (SNPs) in the FSH receptor (FSHR) gene influence the sensitivity of the receptor to FSH.]. 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:18430895
;
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:NP542502.RAIGxhyiegn4RX3TEej5bxw-BGpe0i5qEtz9EnehqwTpc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:27+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" .
}