@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI
> .
@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:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_head
{
this:
np:hasAssertion
dgn-np:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_assertion
;
np:hasProvenance
dgn-np:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_provenance
;
np:hasPublicationInfo
dgn-np:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_assertion
a
np:Assertion
.
dgn-np:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_provenance
a
np:Provenance
.
dgn-np:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_assertion
{
miriam-gene:10249
a
ncit:C16612
.
lld:C0007130
a
ncit:C7057
.
dgn-gda:DGN9d5ef82ad1554063c314e03d438c41a0
sio:SIO_000628
miriam-gene:10249
,
lld:C0007130
;
a
sio:SIO_001121
.
}
dgn-np:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_provenance
{
dgn-np:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_assertion
dcterms:description
"[Although GTT mutation in codon 12 was predominantly observed in adenocarcinoma (10 of 11), GAT mutation (12 of 33) was as frequent as GTT mutation (11 of 33) in ACF together with mutation at codon 13 (7 of 33).]. 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:7889486
;
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:NP752513.RA6zFo7banER8aQiSjCVnsWf6rVPDpEPi27ae6JcFAcMI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}