@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk
> .
@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:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_head
{
this:
np:hasAssertion
dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_assertion
;
np:hasProvenance
dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_assertion
a
np:Assertion
.
dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_provenance
a
np:Provenance
.
dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0936016
a
ncit:C7057
.
dgn-gda:DGN35fe864b12eca46d8e009ab52264f0d8
sio:SIO_000628
miriam-gene:367
,
lld:C0936016
;
a
sio:SIO_001121
.
}
dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_provenance
{
dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_assertion
dcterms:description
"[This review discusses the various AR gene mutations found in androgen insensitivity syndrome (AIS) and the other conditions described above, and relates how different mutations, or disruption of different functional domains, contributes to the various phenotypes.]. 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:7489816
;
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:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:39+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" .
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pav:version
"v4.0.0" .
}