@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0
> .
@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:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_head
{
this:
np:hasAssertion
dgn-np:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_assertion
;
np:hasProvenance
dgn-np:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_provenance
;
np:hasPublicationInfo
dgn-np:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_assertion
a
np:Assertion
.
dgn-np:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_provenance
a
np:Provenance
.
dgn-np:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_assertion
{
miriam-gene:3623
a
ncit:C16612
.
lld:C0085215
a
ncit:C7057
.
dgn-gda:DGN6c1a5e8c317276fc33200beb48f568e5
sio:SIO_000628
miriam-gene:3623
,
lld:C0085215
;
a
sio:SIO_001121
.
}
dgn-np:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_provenance
{
dgn-np:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_assertion
dcterms:description
"[The identification of an autosomal mutation in the inhibin alpha subunit gene that is significantly linked to POF in certain ethnic populations highlights the role of inhibin in the regulation of ovarian biology and fertility.]. 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:19752047
;
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:NP413130.RAjGjUm4dpAFEqj81TJTlvLMuAmnSbQhWv_dNM2Fa2LL0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}