@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY
> .
@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:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_head
{
this:
np:hasAssertion
dgn-np:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_assertion
;
np:hasProvenance
dgn-np:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_provenance
;
np:hasPublicationInfo
dgn-np:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_assertion
a
np:Assertion
.
dgn-np:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_provenance
a
np:Provenance
.
dgn-np:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_assertion
{
miriam-gene:2516
a
ncit:C16612
.
lld:C0232939
a
ncit:C7057
.
dgn-gda:DGN191685b1350a1219b52bf38f44d73b68
sio:SIO_000628
miriam-gene:2516
,
lld:C0232939
;
a
sio:SIO_001121
.
}
dgn-np:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_provenance
{
dgn-np:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_assertion
dcterms:description
"[This work underlines the need to systematically analyze the SF1 sequence in girls with primary amenorrhea due to 46,XY DSD and low testosterone, as well as in newborns with 46,XY 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:20302644
;
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:NP565243.RALN9NOFRn0oGp7OPq4tXYgedefpQZQ4CjgTmosT4oqzY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}