@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948
> .
@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:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_head
{
this:
np:hasAssertion
dgn-np:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_assertion
;
np:hasProvenance
dgn-np:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_provenance
;
np:hasPublicationInfo
dgn-np:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_assertion
a
np:Assertion
.
dgn-np:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_provenance
a
np:Provenance
.
dgn-np:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C2359469
a
ncit:C7057
.
dgn-gda:DGNb7e44544ffe7771a83309ce1613c0445
sio:SIO_000628
miriam-gene:367
,
lld:C2359469
;
a
sio:SIO_001121
.
}
dgn-np:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_provenance
{
dgn-np:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_assertion
dcterms:description
"[Although CAIS is the best known phenotype, recent studies from our laboratory and elsewhere show that malfunction of the AR is associated with many androgen-regulated diseases or conditions that cross traditional clinical disciplines ranging from paediatrics (ambiguous genitalia), gynaecology (primary amenorrhoea), urology (prostate cancer), neurology (spinal bulbar muscular atrophy), reproductive medicine (male infertility), orthopedics (rheumatoid arthritis), oncology (breast cancer) and dermatology (hirsutism, baldness and acne).]. 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:10711573
;
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:NP782778.RA1La6rD7sJch2Wf4OsfBjzFapvAXkynoXatqz5Sq4948130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}