@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU
> .
@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:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_head
{
this:
np:hasAssertion
dgn-np:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_assertion
;
np:hasProvenance
dgn-np:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_provenance
;
np:hasPublicationInfo
dgn-np:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_assertion
a
np:Assertion
.
dgn-np:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_provenance
a
np:Provenance
.
dgn-np:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_assertion
{
miriam-gene:7905
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN08ee1bd27f9618e4bee42c2ce5dba664
sio:SIO_000628
miriam-gene:7905
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_provenance
{
dgn-np:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_assertion
dcterms:description
"[DNA from 61 primary Ewing tumors and 11 Ewing tumor cell lines was extracted and microsatellite analysis for the detection of instability or loss of heterozygosity was performed for the five markers of the Bethesda panel BAT25, BAT26, D5S346, D2S123, and D17S250, which represents the established marker panel for the analysis of hereditary non-polyposis colorectal carcinoma (HNPCC) 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:17530287
;
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:NP563096.RAIHJA7Mtg7vnaKkk3m37rBcimnWtQ_qWckKmBewDRBzU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}