@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E
> .
@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:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_head
{
this:
np:hasAssertion
dgn-np:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_assertion
;
np:hasProvenance
dgn-np:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_provenance
;
np:hasPublicationInfo
dgn-np:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_assertion
a
np:Assertion
.
dgn-np:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_provenance
a
np:Provenance
.
dgn-np:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_assertion
{
miriam-gene:7832
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN7673a18207e9f77b398dd6b1502e669b
sio:SIO_000628
miriam-gene:7832
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_provenance
{
dgn-np:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_assertion
dcterms:description
"[N- and K-ras mutations at codons 12 and 13 were investigated using oligonucleotide hybridization analysis after PCR amplification and subsequent sequence analysis of the amplified DNA from the region of interest in the following prostatic primary and metastatic (met) carcinoma-derived cell lines: 1013L (primary), PC3 (bone met), DU145 (brain met), and LNCaP (lymph node met).]. 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:7678540
;
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:NP478067.RA1a1UMZ1phASe5YzVY94mDPZ366c-hzctG-G1gl1la7E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:46+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" .
}