@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_head
{
this:
np:hasAssertion
dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_assertion
;
np:hasProvenance
dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_provenance
;
np:hasPublicationInfo
dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_assertion
a
np:Assertion
.
dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_provenance
a
np:Provenance
.
dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_assertion
{
miriam-gene:2661
a
ncit:C16612
.
lld:C0032460
a
ncit:C7057
.
dgn-gda:DGN01bec970d15c954f80bdf49fafceed98
sio:SIO_000628
miriam-gene:2661
,
lld:C0032460
;
a
sio:SIO_001121
.
}
dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_provenance
{
dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_assertion
dcterms:description
"[Fourteen mutations in human (h) GDF9 have been reported in women with premature ovarian failure or polycystic ovarian syndrome as well as in mothers of dizygotic twins, implicating GDF9 in the etiology of these conditions.]. 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:24438375
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:45+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}