@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI
> .
@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:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_head
{
this:
np:hasAssertion
dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_assertion
;
np:hasProvenance
dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_provenance
;
np:hasPublicationInfo
dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_assertion
a
np:Assertion
.
dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_provenance
a
np:Provenance
.
dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN68cd1b76d86d4489c0d684689cf48276
sio:SIO_000628
miriam-gene:4436
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_provenance
{
dgn-np:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_assertion
dcterms:description
"[To clarify the extent of BRAF mutations in HNPCC colorectal carcinomas, which are typical mismatch repair deficient carcinomas, we compared the frequency of BRAF mutations between HNPCC, familial adenomatous polyposis (FAP) and sporadic cases.]. 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:15194222
;
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:NP288178.RALzCAz9zscc7hNpbCj2UGAfkHfwMW5gT4cvgs8oeB5dI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:44+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" .
}