@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ
> .
@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:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_head
{
this:
np:hasAssertion
dgn-np:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_assertion
;
np:hasProvenance
dgn-np:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_assertion
a
np:Assertion
.
dgn-np:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_provenance
a
np:Provenance
.
dgn-np:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_assertion
{
miriam-gene:7173
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNcc971ebbf2b9d3ff68bbcc5bea966485
sio:SIO_000628
miriam-gene:7173
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_provenance
{
dgn-np:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_assertion
dcterms:description
"[Fluorescent MSA was performed with a total of 17 polymorphic markers from chromosomal regions 5q, 8p, 9p, 9q, 13q, 14q, 17p, 17q, and 20q in the 58 cancer specimens as well as in specimens from 20 healthy controls.]. 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:15251942
;
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:NP537159.RA8dkDQkB0eyHOVBr_KFER_1n9DlthPqWIUyaZH8WdqxQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}