@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4
> .
@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:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_head
{
this:
np:hasAssertion
dgn-np:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_assertion
;
np:hasProvenance
dgn-np:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_provenance
;
np:hasPublicationInfo
dgn-np:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_assertion
a
np:Assertion
.
dgn-np:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_provenance
a
np:Provenance
.
dgn-np:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_assertion
{
miriam-gene:10534
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN68cf8744f12d0fe143e00f87cae0020e
sio:SIO_000628
miriam-gene:10534
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_provenance
{
dgn-np:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_assertion
dcterms:description
"[The identification of key molecular alteration cells implicates carcinogen defenses, including GSTP1, growth factor signaling pathways (such as PTEN and p27) and androgens as critical determinants of the phenotype of PCa.]. 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:15045584
;
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:NP689646.RAoiWd8hzNQILtaBTOT9yKEVw22FH7GoYE-rsbqJFw5-4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}