@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE
> .
@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:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_head
{
this:
np:hasAssertion
dgn-np:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_assertion
;
np:hasProvenance
dgn-np:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_provenance
;
np:hasPublicationInfo
dgn-np:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_assertion
a
np:Assertion
.
dgn-np:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_provenance
a
np:Provenance
.
dgn-np:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN447cf7d94c4d7e9c5306a42832792dd3
sio:SIO_000628
miriam-gene:324
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_provenance
{
dgn-np:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_assertion
dcterms:description
"[ Our findings of increased serum t3 level with the APC I1307K allele in prostate cancer patients is not surprising, given the mitogenic potential of t3. Further studies may clarify whether t3 elevation is the mechanism whereby APC gene mutations increase the risk of prostate cancer, or whether other pathophysiologic abnormalities are involved.]. 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:12856637
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48550.RALFwyP74-sPpH6c6v7Hl__OxrCoD9Z2bTMblVIF3JsPE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}