@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q
> .
@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:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_head
{
this:
np:hasAssertion
dgn-np:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_assertion
;
np:hasProvenance
dgn-np:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_assertion
a
np:Assertion
.
dgn-np:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_provenance
a
np:Provenance
.
dgn-np:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_assertion
{
miriam-gene:6716
a
ncit:C16612
.
lld:C1704272
a
ncit:C7057
.
dgn-gda:DGNbe04cbe124c76fd1055b3c0d413268e2
sio:SIO_000628
miriam-gene:6716
,
lld:C1704272
;
a
sio:SIO_001121
.
}
dgn-np:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_provenance
{
dgn-np:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_assertion
dcterms:description
"[We have analyzed the complete coding region of the SRD5A2 gene in 87 histologically confirmed prostate cancer (PC) patients, 40 benign prostatic hyperplasia (BPH) cases, and 96 control samples from southern parts of India.]. 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:19443907
;
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:NP900748.RAN_7MKJeL5ry8ShTpBGqi2URHpVW632pintjm8_jnb4Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:13+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" .
}