@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M
> .
@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:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_head
{
this:
np:hasAssertion
dgn-np:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_assertion
;
np:hasProvenance
dgn-np:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_provenance
;
np:hasPublicationInfo
dgn-np:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_assertion
a
np:Assertion
.
dgn-np:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_provenance
a
np:Provenance
.
dgn-np:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0039585
a
ncit:C7057
.
dgn-gda:DGN213e8064d0bc1dd1270aba0bd67a3faa
sio:SIO_000628
miriam-gene:367
,
lld:C0039585
;
a
sio:SIO_001122
.
}
dgn-np:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_provenance
{
dgn-np:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_assertion
dcterms:description
"[In a Chinese family affected with androgen insensitivity syndrome, the familial distinct feature is that all patients shared an identical Arg840Cys substitution in the AR but displayed high phenotypic variation in disorders of male sexual development ]. 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:17538927
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP153402.RAVpkvXhDRgBsMcEC--orQF8SOyKwhEcl8SFohsUqdt2M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:21+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" .
}