@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg
> .
@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:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_head
{
this:
np:hasAssertion
dgn-np:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_assertion
;
np:hasProvenance
dgn-np:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_provenance
;
np:hasPublicationInfo
dgn-np:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_assertion
a
np:Assertion
.
dgn-np:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_provenance
a
np:Provenance
.
dgn-np:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_assertion
{
miriam-gene:2618
a
ncit:C16612
.
lld:C0039585
a
ncit:C7057
.
dgn-gda:DGN807c97c52fb46e07733efb98c6e38ad4
sio:SIO_000628
miriam-gene:2618
,
lld:C0039585
;
a
sio:SIO_001121
.
}
dgn-np:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_provenance
{
dgn-np:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_assertion
dcterms:description
"[The prevalence of AIS has been estimated to be one case in every 20,000 to 64,000 newborn males for the complete syndrome (CAIS), and the prevalence is unknown for the partial syndrome (PAIS).]. 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:22812659
;
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:NP170902.RApb12vrfB4-cfdJtoazofMNCvLsM5tsd29mJGdhB6kcg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}