@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_head
{
this:
np:hasAssertion
dgn-np:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_assertion
;
np:hasProvenance
dgn-np:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_provenance
;
np:hasPublicationInfo
dgn-np:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_assertion
a
np:Assertion
.
dgn-np:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_provenance
a
np:Provenance
.
dgn-np:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN99fc12e2fb2571d8479dc51b84398229
sio:SIO_000628
miriam-gene:7157
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_provenance
{
dgn-np:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_assertion
dcterms:description
"[K-ras and p53 gene mutations were the most frequent alterations observed in stool from patients with colorectal cancer, but DNA amplification was even more frequent, being present in more than half of patients.]. 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:15017656
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP435478.RAi2tx2Ty1HIyr3ZbzQkuXgOWwNzrAELQNs3IdkRFSveg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:02+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}