@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M
> .
@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:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_head
{
this:
np:hasAssertion
dgn-np:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_assertion
;
np:hasProvenance
dgn-np:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_provenance
;
np:hasPublicationInfo
dgn-np:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_assertion
a
np:Assertion
.
dgn-np:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_provenance
a
np:Provenance
.
dgn-np:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_assertion
{
miriam-gene:2158
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN1805f7863ff9f20351c420635736c3d0
sio:SIO_000628
miriam-gene:2158
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_provenance
{
dgn-np:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_assertion
dcterms:description
"[The differences in the prevalence of BRAF(T1796A) mutations between childhood and adult cases of PTC may well reflect inherent differences in the clinical features of these cancers between the two age groups.]. 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:15356022
;
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:NP212666.RAqoJ5RpyxbWgkP_j6kWWc_QqWZ-wxGtwm7X0i0AcmH7M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:58+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" .
}