@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8
> .
@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:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_head
{
this:
np:hasAssertion
dgn-np:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_assertion
;
np:hasProvenance
dgn-np:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_provenance
;
np:hasPublicationInfo
dgn-np:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_assertion
a
np:Assertion
.
dgn-np:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_provenance
a
np:Provenance
.
dgn-np:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_assertion
{
miriam-gene:27352
a
ncit:C16612
.
lld:C1275081
a
ncit:C7057
.
dgn-gda:DGN9cf17a01f2c6cb13758e51ced00c01eb
sio:SIO_000628
miriam-gene:27352
,
lld:C1275081
;
a
sio:SIO_001121
.
}
dgn-np:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_provenance
{
dgn-np:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_assertion
dcterms:description
"[The recent discoveries of germline HRAS mutations in patients with Costello syndrome and mutations in BRAF, MEK1, and MEK2 in CFC syndrome uncovered the biologic mechanism for the shared phenotypic findings based on the close interaction of the affected gene products within the MAP kinase 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:17551924
;
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:NP613806.RA5QMe1KMAcDAXelb-IYLxotFx9eQsQ1LszXOj_B_t3a8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:23+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" .
}