@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM
> .
@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:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_head
{
this:
np:hasAssertion
dgn-np:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_assertion
;
np:hasProvenance
dgn-np:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_provenance
;
np:hasPublicationInfo
dgn-np:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_assertion
a
np:Assertion
.
dgn-np:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_provenance
a
np:Provenance
.
dgn-np:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_assertion
{
miriam-gene:1048
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGNbc8887af2bb9b78bd9055e42df46bde6
sio:SIO_000628
miriam-gene:1048
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_provenance
{
dgn-np:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_assertion
dcterms:description
"[h-CEA and l-CYFRA 21-1 may be prognostic and predictive serum markers for higher response and longer survival in patients with advanced NSCLC receiving gefitinib or erlotinib, especially in patients with unknown EGFR mutation status or patients with squamous cell carcinoma.]. 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:22869475
;
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:NP654077.RAN1qUlYNBhtylP4WkBJwC0jHccN9747TrxeoM2Th0GJM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:34+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" .
}