@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs
> .
@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:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_head
{
this:
np:hasAssertion
dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_assertion
;
np:hasProvenance
dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_provenance
;
np:hasPublicationInfo
dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_assertion
a
np:Assertion
.
dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_provenance
a
np:Provenance
.
dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0936016
a
ncit:C7057
.
dgn-gda:DGN61a9591bee3abc4257b560d21112bb54
sio:SIO_000628
miriam-gene:367
,
lld:C0936016
;
a
sio:SIO_001121
.
}
dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_provenance
{
dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_assertion
dcterms:description
"[When the mutation of the androgen receptor gene has not been identified, Hind III polymorphism of the trophoblastic DNA is useful in the prenatal diagnosis of androgen insensitivity syndrome in high-risk families.]. 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:7910529
;
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:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:47+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" .
}