@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0
> .
@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/v4.0.0/void/
> .
dgn-np:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_head
{
this:
np:hasAssertion
dgn-np:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_assertion
;
np:hasProvenance
dgn-np:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_provenance
;
np:hasPublicationInfo
dgn-np:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_assertion
a
np:Assertion
.
dgn-np:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_provenance
a
np:Provenance
.
dgn-np:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNe2e61e5aea25598c087df23c2c2c1a62
sio:SIO_000628
miriam-gene:1029
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_provenance
{
dgn-np:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_assertion
dcterms:description
"[Since germline mutations in the exons of CDKN2A are rare, it is likely that variants in the noncoding regions of this gene, or in another gene nearby, are responsible for this major determinant of moliness and, hence, of melanoma risk.]. 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:10417291
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP258433.RAkCOICeriU8cJqoiVt5utZDLbRi-iAmkcymuPEfzamK0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:43+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}