@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw
> .
@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:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_head
{
this:
np:hasAssertion
dgn-np:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_assertion
;
np:hasProvenance
dgn-np:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_provenance
;
np:hasPublicationInfo
dgn-np:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_assertion
a
np:Assertion
.
dgn-np:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_provenance
a
np:Provenance
.
dgn-np:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_assertion
{
miriam-gene:6046
a
ncit:C16612
.
lld:C0018418
a
ncit:C7057
.
dgn-gda:DGN251baab8bff29bbb09fc08b9c0191cc2
sio:SIO_000628
miriam-gene:6046
,
lld:C0018418
;
a
sio:SIO_001121
.
}
dgn-np:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_provenance
{
dgn-np:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_assertion
dcterms:description
"[The authors suggest that male patients presenting with gynaecomastia in puberty, and elevated circulating levels of testosterone, estradiol and LH in puberty, but normal FSH, should be suspected of having PAIS and undergo genetic testing for AR mutations.]. 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:22412043
;
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:NP843998.RA40DrNBGrp4nffu72_zYdteamSrTpvmE_IvRJFQmENHw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:36+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" .
}