@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY
> .
@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:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_head
{
this:
np:hasAssertion
dgn-np:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_assertion
;
np:hasProvenance
dgn-np:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_provenance
;
np:hasPublicationInfo
dgn-np:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_assertion
a
np:Assertion
.
dgn-np:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_provenance
a
np:Provenance
.
dgn-np:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_assertion
{
miriam-gene:5727
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN6b7df1f5544a174d5986b04fd6c84cdf
sio:SIO_000628
miriam-gene:5727
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_provenance
{
dgn-np:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_assertion
dcterms:description
"[In several other tumor types, somatic inactivating PTCH1 mutations have been shown to lead to aberrant Hedgehog signaling, but in colorectal cancer the role of PTCH1 mutations has not been thoroughly studied.]. 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:21234763
;
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:NP452677.RA92vUKlMb0jmQNXTssLsFTsIYvdjTN7m_7vCpBIFpQsY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:30+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" .
}