@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA
> .
@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:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_head
{
this:
np:hasAssertion
dgn-np:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_assertion
;
np:hasProvenance
dgn-np:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_provenance
;
np:hasPublicationInfo
dgn-np:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_assertion
a
np:Assertion
.
dgn-np:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_provenance
a
np:Provenance
.
dgn-np:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_assertion
{
miriam-gene:3815
a
ncit:C16612
.
lld:C1336708
a
ncit:C7057
.
dgn-gda:DGN4ca7777c54923623ebf847b3d7dbe113
sio:SIO_000628
miriam-gene:3815
,
lld:C1336708
;
a
sio:SIO_001121
.
}
dgn-np:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_provenance
{
dgn-np:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_assertion
dcterms:description
"[KITLG, encoding the ligand for the receptor tyrosine kinase KIT, which has previously been implicated in the pathogenesis of TGCT and the biology of germ cells, may explain the association on chromosome 12.]. 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:19483681
;
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:NP690278.RAOdlG61qdQ5dvKIzKh8e865RCaqdbAQ5OCxw4Q4nQbuA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}