@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8
> .
@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:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_head
{
this:
np:hasAssertion
dgn-np:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_assertion
;
np:hasProvenance
dgn-np:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_provenance
;
np:hasPublicationInfo
dgn-np:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_assertion
a
np:Assertion
.
dgn-np:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_provenance
a
np:Provenance
.
dgn-np:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGNcb4009c9a721f2420f2d0f2053f22faa
sio:SIO_000628
miriam-gene:4771
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_provenance
{
dgn-np:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_assertion
dcterms:description
"[The identification of chromosomal aberrations in patients with NF2 that involve chromosome 22 will play an important role in the identification of the NF2 gene in much the same way as they have in NF1.]. 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:1669691
;
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:NP797957.RA9Sa4EXCGZ9TRGQZamBvnx2o5aKvMDv8tny3Mu2JowK8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}