@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ
> .
@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:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_head
{
this:
np:hasAssertion
dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_assertion
;
np:hasProvenance
dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_assertion
a
np:Assertion
.
dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_provenance
a
np:Provenance
.
dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN2cd9df828b31e6af9ac70a37d2cdf9cd
sio:SIO_000628
miriam-gene:2153
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_provenance
{
dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_assertion
dcterms:description
"[This study shows that for some genes, further studies are unnecessary, whereas for others, no more enrollments are needed. The impact of certain genotypes must be examined in relation to other established risk factors and potentially new therapeutic strategies.]. 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:11397354
;
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:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}