@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc
> .
@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:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_head
{
this:
np:hasAssertion
dgn-np:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_assertion
;
np:hasProvenance
dgn-np:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_provenance
;
np:hasPublicationInfo
dgn-np:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_assertion
a
np:Assertion
.
dgn-np:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_provenance
a
np:Provenance
.
dgn-np:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_assertion
{
miriam-gene:1589
a
ncit:C16612
.
lld:C0041408
a
ncit:C7057
.
dgn-gda:DGNb1973c673155f49ad5ade8ef02976306
sio:SIO_000628
miriam-gene:1589
,
lld:C0041408
;
a
sio:SIO_001121
.
}
dgn-np:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_provenance
{
dgn-np:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_assertion
dcterms:description
"[Southern-blotting studies and PCR analyses of SRY, androgen receptor and CYP21B genes can be routinely used for the direct diagnosis of gonadal dysgenesis, androgen insensitivity syndromes and congenital adrenal hyperplasia, respectively.]. 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:1306840
;
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:NP673132.RAITi7wnYA4j5e7VVNp-n8uG7lQzOJiD9blNq5xwldXSc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}