@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI
> .
@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:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_head
{
this:
np:hasAssertion
dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_assertion
;
np:hasProvenance
dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_assertion
a
np:Assertion
.
dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_provenance
a
np:Provenance
.
dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_assertion
{
miriam-gene:960
a
ncit:C16612
.
lld:C0233643
a
ncit:C7057
.
dgn-gda:DGN48a5a141f573ca4ac8ab402401712b40
sio:SIO_000628
miriam-gene:960
,
lld:C0233643
;
a
sio:SIO_001121
.
}
dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_provenance
{
dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_assertion
dcterms:description
"[This fact and the huge potential number of different CD44 splice variants that can contain v3 and v6 domains can explain incoherence of clinical studies regarding functional asessment of CD44 variants, as well as diminish the chances of using CD44 variants for predictive purpose.]. 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:23151220
;
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:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:29+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" .
}