@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_head
{
this:
np:hasAssertion
dgn-np:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_assertion
;
np:hasProvenance
dgn-np:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_provenance
;
np:hasPublicationInfo
dgn-np:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_assertion
a
np:Assertion
.
dgn-np:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_provenance
a
np:Provenance
.
dgn-np:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_assertion
{
miriam-gene:7852
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN5c70f9e428b95c150af3d71af596a861
sio:SIO_000628
miriam-gene:7852
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_provenance
{
dgn-np:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_assertion
dcterms:description
"[CXCR4 somatic mutations in WM are the first ever reported in human cancer and are similar to nonsense (NS) and frameshift (FS) germline mutations found in warts, hypogammaglobulinemia, infections and myelokathexis (WHIM) syndrome.]. 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:24553177
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP784455.RAoFO0gzPw_kEy4epRRacdhL0_69zwfayoM5UZq2AagmM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:34+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}