@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0
> .
@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:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_head
{
this:
np:hasAssertion
dgn-np:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_assertion
;
np:hasProvenance
dgn-np:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_provenance
;
np:hasPublicationInfo
dgn-np:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_assertion
a
np:Assertion
.
dgn-np:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_provenance
a
np:Provenance
.
dgn-np:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_assertion
{
miriam-gene:5789
a
ncit:C16612
.
lld:C2939420
a
ncit:C7057
.
dgn-gda:DGNfdc3a174c56a2dfbb37b18c2eb4ac7c0
sio:SIO_000628
miriam-gene:5789
,
lld:C2939420
;
a
sio:SIO_001121
.
}
dgn-np:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_provenance
{
dgn-np:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_assertion
dcterms:description
"[Combined with the high mutation rate observed in our study, PTPRD is one of the most commonly altered genes in cSCC and warrants further investigation to determine its significance for metastasis in other tumor types.]. 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:22052591
;
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:NP343434.RAWrwYNG_UXrxtTihrAuPwyl0yAbhdRLLwtENt4cb_kc0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}