@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4
> .
@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:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_head
{
this:
np:hasAssertion
dgn-np:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_assertion
;
np:hasProvenance
dgn-np:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_provenance
;
np:hasPublicationInfo
dgn-np:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_assertion
a
np:Assertion
.
dgn-np:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_provenance
a
np:Provenance
.
dgn-np:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_assertion
{
miriam-gene:7063
a
ncit:C16612
.
lld:C0206704
a
ncit:C7057
.
dgn-gda:DGN8fc2bc8643b77f80d870a38bf8b70da4
sio:SIO_000628
miriam-gene:7063
,
lld:C0206704
;
a
sio:SIO_001121
.
}
dgn-np:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_provenance
{
dgn-np:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_assertion
dcterms:description
"[Occasional point mutations in ras oncogenes were detected in adenosquamous carcinomas (one of five cases) and large cell carcinoma (one of 24 cases), but no ras activations were found in small cell carcinomas (six cases), squamous carcinomas (48 cases), carcinoid carcinomas (15 cases), or thymoma (one case).]. 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:1562997
;
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:NP938434.RAZggfA8Aqm9ecJly3OUoUcStDW1ce-42YQgUAt0S_Pf4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}