@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q
> .
@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:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_head
{
this:
np:hasAssertion
dgn-np:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_assertion
;
np:hasProvenance
dgn-np:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_assertion
a
np:Assertion
.
dgn-np:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_provenance
a
np:Provenance
.
dgn-np:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0152013
a
ncit:C7057
.
dgn-gda:DGN529513b97bb8f94164a63e12000ea7df
sio:SIO_000628
miriam-gene:3845
,
lld:C0152013
;
a
sio:SIO_001121
.
}
dgn-np:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_provenance
{
dgn-np:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_assertion
dcterms:description
"[The paradigms are EGFR mutations in adenocarcinoma of the lung that can be treated with gefitinib, KRAS mutations in colon cancer with respect to treatment with EGFR antibodies, and the use of gene-expression analysis for ER-positive, node-negative breast cancer patients with respect to chemotherapy options.]. 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:20351699
;
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:NP326612.RAtmyc6iOOeOZtftDmgZ-o_Uh7JT2VJZvuZVlBrd_Gv0Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:11+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" .
}