@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ
> .
@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:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_head
{
this:
np:hasAssertion
dgn-np:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_assertion
;
np:hasProvenance
dgn-np:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_assertion
a
np:Assertion
.
dgn-np:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_provenance
a
np:Provenance
.
dgn-np:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_assertion
{
miriam-gene:2492
a
ncit:C16612
.
lld:C0085083
a
ncit:C7057
.
dgn-gda:DGNcbfecd668a140425c04f0eb5c148bffa
sio:SIO_000628
miriam-gene:2492
,
lld:C0085083
;
a
sio:SIO_001121
.
}
dgn-np:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_provenance
{
dgn-np:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_assertion
dcterms:description
"[Beside point mutations, FSHR gene polymorphisms at specific sites (e.g., codons 307 and 680) may influence FSHR protein responsiveness to exogenous FSH, and finally affect the effectiveness of in vitro fertilization (IVF) treatment as well as the likelihood of developing a severe OHSS as a consequence of superovulation.]. 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:19017414
;
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:NP526322.RAldBer_PkGKucnIBS127zux-90KRm2odGW7LjG0_BQbQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}