@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE
> .
@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:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_head
{
this:
np:hasAssertion
dgn-np:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_assertion
;
np:hasProvenance
dgn-np:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_provenance
;
np:hasPublicationInfo
dgn-np:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_assertion
a
np:Assertion
.
dgn-np:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_provenance
a
np:Provenance
.
dgn-np:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0346647
a
ncit:C7057
.
dgn-gda:DGN550a08383ab33ba6f3e538539f2287c1
sio:SIO_000628
miriam-gene:1029
,
lld:C0346647
;
a
sio:SIO_001122
.
}
dgn-np:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_provenance
{
dgn-np:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_assertion
dcterms:description
"[The presence of a deletion including exon 1B in two PC patients points to the involvement of p14(ARF) in the development of PC and may suggest that the increased risk of PC in MF is caused by impairment of both loci.]. 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:14679123
;
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:NP59764.RAM4zH1ZXbgueQQtPxCXnzljtp_538MzVKA6Wjp6_NBbE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}