@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w
> .
@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:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_head
{
this:
np:hasAssertion
dgn-np:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_assertion
;
np:hasProvenance
dgn-np:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_provenance
;
np:hasPublicationInfo
dgn-np:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_assertion
a
np:Assertion
.
dgn-np:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_provenance
a
np:Provenance
.
dgn-np:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_assertion
{
miriam-gene:728695
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN45f1adde2ba6ec87d7de146e27085e36
sio:SIO_000628
miriam-gene:728695
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_provenance
{
dgn-np:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_assertion
dcterms:description
"[The incidence of melanoma has dramatically increased in many countries (it is 4.5 cases every 100 000 inhabitants in Sicily) and Xq27 region contains genes important in cancer like the SPANX (sperm protein associated with the nucleus in the X chromosome) gene family.]. 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:18626316
;
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:NP716639.RA0NJWsDe2ub8q5WDow-p5PBM-QSOpwTuWeGvNYqowM_w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:15+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" .
}