@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM
> .
@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:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_head
{
this:
np:hasAssertion
dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_assertion
;
np:hasProvenance
dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_provenance
;
np:hasPublicationInfo
dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_assertion
a
np:Assertion
.
dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_provenance
a
np:Provenance
.
dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_assertion
{
miriam-gene:2492
a
ncit:C16612
.
lld:C0021361
a
ncit:C7057
.
dgn-gda:DGNb4a2fda3d2a2c1f6a6aeafdbbc1fe811
sio:SIO_000628
miriam-gene:2492
,
lld:C0021361
;
a
sio:SIO_001122
.
}
dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_provenance
{
dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_assertion
dcterms:description
"[ The results show that Ser/Ser-680 predominates in the studied infertile population. Furthermore, women with normal ovarian reserve and the Ser/Ser FSH receptor variant had significantly higher FSH levels, compared to women with Asn/Asn and Asn/Ser variants. FSH receptor genotyping may, thus, be interesting as an adjunct indicator of ovarian reserve for infertile women undergoing assisted reproduction, and may be helpful in the determination of the starting dosage of FSH in in vitro fertilization.]. 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:16026410
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}