@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw
> .
@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:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_head
{
this:
np:hasAssertion
dgn-np:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_assertion
;
np:hasProvenance
dgn-np:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_provenance
;
np:hasPublicationInfo
dgn-np:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_assertion
a
np:Assertion
.
dgn-np:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_provenance
a
np:Provenance
.
dgn-np:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_assertion
{
miriam-gene:4254
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNe020b958f778264dd01ae4c467679d42
sio:SIO_000628
miriam-gene:4254
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_provenance
{
dgn-np:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_assertion
dcterms:description
"[Although most variants are cancer specific, pleiotropy has been observed for several variants, for example, variants at the 8q24 locus and breast, ovarian and prostate cancers or variants in KITLG in relation to hair color and testicular cancer.]. 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:21459759
;
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:NP396004.RAxLS_6NrHONNBaTaV0bBf86nDIvdBhnWgGx-9QlHAocw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}