@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc
> .
@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:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_head
{
this:
np:hasAssertion
dgn-np:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_assertion
;
np:hasProvenance
dgn-np:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_provenance
;
np:hasPublicationInfo
dgn-np:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_assertion
a
np:Assertion
.
dgn-np:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_provenance
a
np:Provenance
.
dgn-np:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_assertion
{
miriam-gene:7133
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN1505bb772b53f6753956067abf9545c4
sio:SIO_000628
miriam-gene:7133
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_provenance
{
dgn-np:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_assertion
dcterms:description
"[The TNFRSF1B genotype did not influence any clinical or biochemical variable related to hyperandrogenism or insulin sensitivity and was not associated with obesity, both in hyperandrogenic patients and healthy controls considered separately.]. 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:12161545
;
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:NP512804.RAjElIeh0KlxOLX34f7sKSTpHAcrI35fQzCvYUIShVghc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}