@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw
> .
@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:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_head
{
this:
np:hasAssertion
dgn-np:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_assertion
;
np:hasProvenance
dgn-np:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_provenance
;
np:hasPublicationInfo
dgn-np:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_assertion
a
np:Assertion
.
dgn-np:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_provenance
a
np:Provenance
.
dgn-np:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_assertion
{
miriam-gene:4233
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGNdc20c9e321e4f682c1bd3709bb0e4689
sio:SIO_000628
miriam-gene:4233
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_provenance
{
dgn-np:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_assertion
dcterms:description
"[The MET (also known as c-met proto-oncogene located at 7q31-34 has been shown to be amplified in human gliomas, and activating mutations within the tyrosine kinase domain of MET have been causally related to tumorigenesis in hereditary papillary renal 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:11007037
;
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:NP316694.RA87IyVCuGgQQTA3ebc6yIser2WIDxwrW-koQERnEzCjw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:03+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" .
}