@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE
> .
@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/v4.0.0/void/
> .
dgn-np:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_head
{
this:
np:hasAssertion
dgn-np:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_assertion
;
np:hasProvenance
dgn-np:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_provenance
;
np:hasPublicationInfo
dgn-np:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_assertion
a
np:Assertion
.
dgn-np:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_provenance
a
np:Provenance
.
dgn-np:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_assertion
{
miriam-gene:1589
a
ncit:C16612
.
lld:C0520463
a
ncit:C7057
.
dgn-gda:DGN8793b226542654ed3d25b0bd8eb215bc
sio:SIO_000628
miriam-gene:1589
,
lld:C0520463
;
a
sio:SIO_001121
.
}
dgn-np:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_provenance
{
dgn-np:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_assertion
dcterms:description
"[Mutation analysis of CYP21A2 gene was performed in seven patients with congenital adrenal hyperplasia (CAH) by combining differential long template polymerase chain reaction (PCR) amplification and amplified created restriction site (ACRS) methods.]. 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:11431859
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP322455.RAbQSiQMyDMm0Ci1vTDMW3Bvc3wQWD5oNlzrh5qCfw3vE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:11+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}