@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI
> .
@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:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_head
{
this:
np:hasAssertion
dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_assertion
;
np:hasProvenance
dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_provenance
;
np:hasPublicationInfo
dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_assertion
a
np:Assertion
.
dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_provenance
a
np:Provenance
.
dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGNaf47a786ad97c6b60483a12a2d986449
sio:SIO_000628
miriam-gene:4771
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_provenance
{
dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_assertion
dcterms:description
"[In order to examine the significance of NF2 in general carcinogenesis, comprehensive analyses of 68 cases of breast carcinoma, which shows frequent loss of heterozygosity at chromosome 22, and 48 hepatocellular carcinomas of different histological grade were performed.]. 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:7877257
;
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:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:34+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" .
}