@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs
> .
@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:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_head
{
this:
np:hasAssertion
dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_assertion
;
np:hasProvenance
dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_provenance
;
np:hasPublicationInfo
dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_assertion
a
np:Assertion
.
dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_provenance
a
np:Provenance
.
dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_assertion
{
miriam-gene:8797
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGNecd89d4121fda08c15d040bd1d43dc97
sio:SIO_000628
miriam-gene:8797
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_provenance
{
dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_assertion
dcterms:description
"[There were significant differences in the frequencies of HLA DR1, DR4 and DR7 between patients who only had basal cell carcinomas and patients who had both basal and squamous cell carcinomas.]. 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:8136554
;
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:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}