@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU
> .
@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:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_head
{
this:
np:hasAssertion
dgn-np:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_assertion
;
np:hasProvenance
dgn-np:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_provenance
;
np:hasPublicationInfo
dgn-np:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_assertion
a
np:Assertion
.
dgn-np:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_provenance
a
np:Provenance
.
dgn-np:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_assertion
{
miriam-gene:23414
a
ncit:C16612
.
lld:C2751824
a
ncit:C7057
.
dgn-gda:DGN7e70a1d838812c40275bfdb2d854c605
sio:SIO_000628
miriam-gene:23414
,
lld:C2751824
;
a
sio:SIO_001121
.
}
dgn-np:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_provenance
{
dgn-np:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_assertion
dcterms:description
"[This is the first example of mutations in the coding sequence of FOG2 associated with 46,XY DSD in human and adds to the list of genes in the human known to be associated with DSD.]. 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:24549039
;
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:NP872430.RA0XgstOppAGv3tZeGl8RgDbANG92vwtPjrsNY7PF4BtU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:31+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" .
}