@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs
> .
@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:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_head
{
this:
np:hasAssertion
dgn-np:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_assertion
;
np:hasProvenance
dgn-np:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_provenance
;
np:hasPublicationInfo
dgn-np:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_assertion
a
np:Assertion
.
dgn-np:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_provenance
a
np:Provenance
.
dgn-np:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGNb6935a6ce74b3449734e81e047d8dd3d
sio:SIO_000628
miriam-gene:2272
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_provenance
{
dgn-np:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_assertion
dcterms:description
"[Taken together, the consistently significant but flipped association between single nucleotide polymorphism rs760317 and prostate cancer in three independent samples suggests that rs760317 may be in linkage disequilibrium with one or more prostate cancer susceptibility variants in or near FHIT.]. 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:17548701
;
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:NP740281.RAvBRYOFSn8bTMxcadVjnUaqykTtSbwwDwt2Du55ZoAKs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+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" .
}