@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho
> .
@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:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_head
{
this:
np:hasAssertion
dgn-np:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_assertion
;
np:hasProvenance
dgn-np:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_provenance
;
np:hasPublicationInfo
dgn-np:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_assertion
a
np:Assertion
.
dgn-np:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_provenance
a
np:Provenance
.
dgn-np:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_assertion
{
miriam-gene:2767
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN3efe3e59b9ffd2205278ec964b6f9339
sio:SIO_000628
miriam-gene:2767
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_provenance
{
dgn-np:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_assertion
dcterms:description
"[Furthermore, this review will also consider some additional mutations in genes such as KIT, GNAQ, and GNA11, which can be seen in certain subtypes of melanoma and whose gene products interact with the MAPK pathway.]. 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:23752084
;
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:NP752741.RAuydldyTVooQgPHwQnpUN8ehpx5schO3gtzWWnZjc3Ho130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}