@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E
> .
@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:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_head
{
this:
np:hasAssertion
dgn-np:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_assertion
;
np:hasProvenance
dgn-np:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_assertion
a
np:Assertion
.
dgn-np:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_provenance
a
np:Provenance
.
dgn-np:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN7b19de97ea573e65978acc13fb536220
sio:SIO_000628
miriam-gene:1029
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_provenance
{
dgn-np:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_assertion
dcterms:description
"[Genetic testing for CDKN2A mutations is currently available but the Melanoma Genetics Consortium recommends offering such testing to patients only in the context of research protocols because clinical utility is uncertain.]. 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:24258989
;
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:NP1130026.RAWuP6wJcuZm2mzKzcHAU5eHLW8MZx3h3l3LDj22mSE3E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:18+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" .
}