@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE
> .
@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:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_head
{
this:
np:hasAssertion
dgn-np:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_assertion
;
np:hasProvenance
dgn-np:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_provenance
;
np:hasPublicationInfo
dgn-np:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_assertion
a
np:Assertion
.
dgn-np:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_provenance
a
np:Provenance
.
dgn-np:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_assertion
{
miriam-gene:6716
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN5b281a218ba2a6f6c1d5ffd1614cbd5f
sio:SIO_000628
miriam-gene:6716
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_provenance
{
dgn-np:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_assertion
dcterms:description
"[In conclusion, our findings do not provide evidence for an important role of the V89L polymorphism in the etiology of breast cancer. However, in breast cancer patients, the LL genotype may be associated with unfavorable prognosis.]. 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:14652280
;
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:NP51076.RAMCqcFKT4DI_zmebBsDQP0GEShB064J1KjNlainDkZLE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}