@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY
> .
@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/v3.0.0/void/
> .
dgn-np:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_head
{
this:
np:hasAssertion
dgn-np:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_assertion
;
np:hasProvenance
dgn-np:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_provenance
;
np:hasPublicationInfo
dgn-np:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_assertion
a
np:Assertion
.
dgn-np:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_provenance
a
np:Provenance
.
dgn-np:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_assertion
{
miriam-gene:4157
a
ncit:C16612
.
lld:C0038814
a
ncit:C7057
.
dgn-gda:DGNbd3d196ed583fb786666fbf173a7c0d6
sio:SIO_000628
miriam-gene:4157
,
lld:C0038814
;
a
sio:SIO_001122
.
}
dgn-np:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_provenance
{
dgn-np:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_assertion
dcterms:description
"[Results show that MC1R variants, hair color, and number of nevi were jointly associated with melanoma risk in CDKN2A mutation carriers. This joint association may have important consequences for risk assessments in familial settings.]. 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:20876876
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP131260.RAJf5b8DdnwxSqc5Xh6dqJclB3i6egp97nZviiqscKilY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:53+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}