@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg
> .
@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:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_head
{
this:
np:hasAssertion
dgn-np:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_assertion
;
np:hasProvenance
dgn-np:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_provenance
;
np:hasPublicationInfo
dgn-np:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_assertion
a
np:Assertion
.
dgn-np:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_provenance
a
np:Provenance
.
dgn-np:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_assertion
{
miriam-gene:2201
a
ncit:C16612
.
lld:C0007133
a
ncit:C7057
.
dgn-gda:DGN5b967f8287226b04f51e205a4518812c
sio:SIO_000628
miriam-gene:2201
,
lld:C0007133
;
a
sio:SIO_001121
.
}
dgn-np:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_provenance
{
dgn-np:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_assertion
dcterms:description
"[Two of five PDC cases and one papillary carcinoma revealed point mutations in exon 8 as follows; GTG (val) to CTG (leu) at codon 272 in case 23T, CGA (arg) to CCA (pro) at codon 306 in case of 30T, and CGG (arg) to AGG (arg) at codon 282 in case 28T.]. 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:8616809
;
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:NP253914.RAEtMMA1RCNKLJv8SgyW7ZHtt56SS7fb_lTtELIVa-lOg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:22+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" .
}