@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs
> .
@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:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_head
{
this:
np:hasAssertion
dgn-np:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_assertion
;
np:hasProvenance
dgn-np:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_provenance
;
np:hasPublicationInfo
dgn-np:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_assertion
a
np:Assertion
.
dgn-np:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_provenance
a
np:Provenance
.
dgn-np:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_assertion
{
miriam-gene:4233
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNb3a443af3c638b940a344e183bb923e4
sio:SIO_000628
miriam-gene:4233
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_provenance
{
dgn-np:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_assertion
dcterms:description
"[The observed spectrum of mutations in resistant cells was dominated by substitutions of tyrosine 1230 but also included other missense mutations and partially overlapped with activating MET mutations that were previously described in cancer 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:21697284
;
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:NP188043.RA-C3LSSdKRZTvf9qRj4UN3J976801xTJAbVndOmImePs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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" .
}