@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q
> .
@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:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_head
{
this:
np:hasAssertion
dgn-np:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_assertion
;
np:hasProvenance
dgn-np:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_assertion
a
np:Assertion
.
dgn-np:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_provenance
a
np:Provenance
.
dgn-np:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_assertion
{
miriam-gene:5706
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN3b20755862a6701e516a47c8487c2b45
sio:SIO_000628
miriam-gene:5706
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_provenance
{
dgn-np:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_assertion
dcterms:description
"[On the basis of our data showing that melanoma iNOS expression predicts shortened patient survival, we formulated the hypothesis that activating mutations of NRAS or BRAF, which lead to constitutive activation of the p44/42 MAPK pathway, drive iNOS expression in human melanoma.]. 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:16474847
;
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:NP293186.RAOkQkKgAH-H5CpiMxuvZFUHuGenHGryKqC9Cfeg0_j_Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}