@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k
> .
@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:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_head
{
this:
np:hasAssertion
dgn-np:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_assertion
;
np:hasProvenance
dgn-np:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_provenance
;
np:hasPublicationInfo
dgn-np:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_assertion
a
np:Assertion
.
dgn-np:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_provenance
a
np:Provenance
.
dgn-np:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C1334274
a
ncit:C7057
.
dgn-gda:DGN53bccc3464fe0f436fbf89c0621d68df
sio:SIO_000628
miriam-gene:673
,
lld:C1334274
;
a
sio:SIO_001121
.
}
dgn-np:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_provenance
{
dgn-np:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_assertion
dcterms:description
"[These findings suggest that BRAF mutations may be associated with the pathogenesis of SSA, but progression to HGD or early invasive carcinoma may be associated with other factors, such as alterations of p53 and β-catenin.]. 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:21263251
;
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:NP725587.RAIkFJZePKST7HErDw_Rgar3yu-9m-F2WEi7Cr74mDg5k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}