@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA
> .
@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:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_head
{
this:
np:hasAssertion
dgn-np:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_assertion
;
np:hasProvenance
dgn-np:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_provenance
;
np:hasPublicationInfo
dgn-np:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_assertion
a
np:Assertion
.
dgn-np:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_provenance
a
np:Provenance
.
dgn-np:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_assertion
{
miriam-gene:5605
a
ncit:C16612
.
lld:C1275081
a
ncit:C7057
.
dgn-gda:DGN77c9d0ca16bd264512c61ee4c5788ecc
sio:SIO_000628
miriam-gene:5605
,
lld:C1275081
;
a
sio:SIO_001121
.
}
dgn-np:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_provenance
{
dgn-np:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP646046.RArvh5wgvDpc8N1mRhhQDSRzUUil4bP3KdiDqRzi8M4VA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:08+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" .
}