@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo
> .
@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:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_head
{
this:
np:hasAssertion
dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_assertion
;
np:hasProvenance
dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_provenance
;
np:hasPublicationInfo
dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_assertion
a
np:Assertion
.
dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_provenance
a
np:Provenance
.
dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_assertion
{
miriam-gene:7864
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGN586d16997197887e1ec23634e69a6540
sio:SIO_000628
miriam-gene:7864
,
lld:C0001418
;
a
sio:SIO_001121
.
}
dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_provenance
{
dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_assertion
dcterms:description
"[The frequency of detection of the A1/A1 genotype in the tumor tissues was increased in adenocarcinoma patients as compared with the blood of adenocarcinoma patients and was decreased in the blood of SCLC patients as compared with the blood of healthy individuals.]. 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:8608979
;
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:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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" .
}