@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg
> .
@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:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_head
{
this:
np:hasAssertion
dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_assertion
;
np:hasProvenance
dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_provenance
;
np:hasPublicationInfo
dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_assertion
a
np:Assertion
.
dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_provenance
a
np:Provenance
.
dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0206702
a
ncit:C7057
.
dgn-gda:DGN215f21d0cd2bab0d6de399be90973278
sio:SIO_000628
miriam-gene:7157
,
lld:C0206702
;
a
sio:SIO_001121
.
}
dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_provenance
{
dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_assertion
dcterms:description
"[The systematic screening for p53 mutations in European patients with hilar cholangiocarcinoma has shown that the type of mutation (except 175) is different and its incidence is much lower when compared to the pattern previously reported for intrahepatic cholangiocarcinoma in East Asian patients.]. 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:10998080
;
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:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:29+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" .
}