@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A
> .
@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:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_head
{
this:
np:hasAssertion
dgn-np:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_assertion
;
np:hasProvenance
dgn-np:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_provenance
;
np:hasPublicationInfo
dgn-np:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_assertion
a
np:Assertion
.
dgn-np:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_provenance
a
np:Provenance
.
dgn-np:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_assertion
{
miriam-gene:6462
a
ncit:C16612
.
lld:C0001973
a
ncit:C7057
.
dgn-gda:DGNcd1c9ff50ad273ba7522b916ea99cd9b
sio:SIO_000628
miriam-gene:6462
,
lld:C0001973
;
a
sio:SIO_001121
.
}
dgn-np:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_provenance
{
dgn-np:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_assertion
dcterms:description
"[This method of detection was used to determine the distribution of SHBG phenotypes in healthy controls of both sexes and in five different pathological conditions characterized by changes in the SHBG level or endocrine disturbances (malignant and benign ovarian neoplasms, hirsutism, liver cirrhosis and alcoholism).]. 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:8088001
;
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:NP812139.RAci6HNuldRWw15-nTknBJd0-Fwplg63PWtv3pfS3M71A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:18+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" .
}