@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM
> .
@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:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_head
{
this:
np:hasAssertion
dgn-np:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_assertion
;
np:hasProvenance
dgn-np:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_provenance
;
np:hasPublicationInfo
dgn-np:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_assertion
a
np:Assertion
.
dgn-np:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_provenance
a
np:Provenance
.
dgn-np:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1509148
a
ncit:C7057
.
dgn-gda:DGNa6203e276fa2c12076b82458b29631fa
sio:SIO_000628
miriam-gene:7157
,
lld:C1509148
;
a
sio:SIO_001121
.
}
dgn-np:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_provenance
{
dgn-np:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_assertion
dcterms:description
"[We investigated 11 cases of SH by immunohistochemistry, fluorescence in situ hybridization, and polymerase chain reaction-based microsatellite and mutational analyses with particular emphasis on possible alterations of microsatellite loci located at tumor suppressor genes (FHIT, p16, Rb, and p53) involved in lung adenocarcinoma genesis and EGFR, HER2, and K-RAS genes.]. 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:17895751
;
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:NP723089.RAHCiNRu0DB9_7I07HqB-scc18tnMFoj-IhwcpG1jxwiM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}