@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8
> .
@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:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_head
{
this:
np:hasAssertion
dgn-np:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_assertion
;
np:hasProvenance
dgn-np:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_provenance
;
np:hasPublicationInfo
dgn-np:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_assertion
a
np:Assertion
.
dgn-np:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_provenance
a
np:Provenance
.
dgn-np:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0206701
a
ncit:C7057
.
dgn-gda:DGNbd8a07748e11dcea4df00343fecfb4dd
sio:SIO_000628
miriam-gene:673
,
lld:C0206701
;
a
sio:SIO_001121
.
}
dgn-np:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_provenance
{
dgn-np:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_assertion
dcterms:description
"[The molecular genetic findings confirm our hypothesis of dual pathways of serous carcinogenesis based on previous analyses of KRAS and BRAF mutations on the same set of cases in which KRAS and BRAF mutations were found in 60% of SBTs and low-grade serous carcinoma but not in high-grade serous carcinomas.]. 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:15644779
;
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:NP386584.RA1HZi9Qjns4sXaA4m2biB9eKcpHY0BKqO4RJjSP7O9N8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:50+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" .
}