@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k
> .
@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:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_head
{
this:
np:hasAssertion
dgn-np:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_assertion
;
np:hasProvenance
dgn-np:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_provenance
;
np:hasPublicationInfo
dgn-np:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_assertion
a
np:Assertion
.
dgn-np:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_provenance
a
np:Provenance
.
dgn-np:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_assertion
{
miriam-gene:1022
a
ncit:C16612
.
lld:C1275081
a
ncit:C7057
.
dgn-gda:DGN49ccb7abd548b74a8e6512d928f87102
sio:SIO_000628
miriam-gene:1022
,
lld:C1275081
;
a
sio:SIO_001121
.
}
dgn-np:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_provenance
{
dgn-np:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_assertion
dcterms:description
"[While there is significant phenotypic overlap among syndromes of the Ras/MAPK pathway, individuals with CS are more likely than individuals with CFC syndrome to present with cutaneous papillomas, palmoplantar keratoderma and full eyebrows, and are less likely to present with ulerythema ophryogenes, keratosis pilaris or multiple naevi.]. 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:22098123
;
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:NP423676.RAQ3u4FwAhVGPkiOurLtRAfDLRGgvN_m9tyqvhygScR_k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}