@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_head
{
this:
np:hasAssertion
dgn-np:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_assertion
;
np:hasProvenance
dgn-np:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_provenance
;
np:hasPublicationInfo
dgn-np:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_assertion
a
np:Assertion
.
dgn-np:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_provenance
a
np:Provenance
.
dgn-np:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_assertion
{
miriam-gene:27286
a
ncit:C16612
.
lld:C0266464
a
ncit:C7057
.
dgn-gda:DGNbee06f76b4b17fb2104a6d61fad548e9
sio:SIO_000628
miriam-gene:27286
,
lld:C0266464
;
a
sio:SIO_001121
.
}
dgn-np:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_provenance
{
dgn-np:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_assertion
dcterms:description
"[There are more than 100 syndromes possibly associated with PMG but mutations in specific genes such as SRPX2, GPR56, TUBB2B, TUBB3, NHEJ1, TUBA1A, TUBA8, and WDR62 have been reported only in a minority of patients.]. 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:24072599
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP887781.RAWq9aPzhmm0NhdzxXrwq28Zsso_bBT2MWjarbaJ1D2_s130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:41+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}