@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk
> .
@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:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_head
{
this:
np:hasAssertion
dgn-np:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_assertion
;
np:hasProvenance
dgn-np:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_provenance
;
np:hasPublicationInfo
dgn-np:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_assertion
a
np:Assertion
.
dgn-np:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_provenance
a
np:Provenance
.
dgn-np:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0001627
a
ncit:C7057
.
dgn-gda:DGNe4e54c8308b59c434ea467050ad70f2f
sio:SIO_000628
miriam-gene:3126
,
lld:C0001627
;
a
sio:SIO_001121
.
}
dgn-np:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_provenance
{
dgn-np:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_assertion
dcterms:description
"[Diagnosis of congenital adrenal hyerplasia in fetuses that are at risk for congenital adrenal hyperplasia can be determined using human leukocyte antigen haplotype or by demonstration of excess cortisol precursors in amniotic fluid.]. 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:10088875
;
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:NP909219.RA7aUsKDfjOQ4yeo5AlJBnYy-R5oei_2BIiP59Y5Cbtbk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:18+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" .
}