@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8
> .
@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:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_head
{
this:
np:hasAssertion
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_assertion
;
np:hasProvenance
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_provenance
;
np:hasPublicationInfo
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_assertion
a
np:Assertion
.
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_provenance
a
np:Provenance
.
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_assertion
{
miriam-gene:57332
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN94d52eac67acae7a953853cb7f083758
sio:SIO_000628
miriam-gene:57332
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_provenance
{
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_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:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:58+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" .
}