@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU
> .
@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:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_head
{
this:
np:hasAssertion
dgn-np:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_assertion
;
np:hasProvenance
dgn-np:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_provenance
;
np:hasPublicationInfo
dgn-np:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_assertion
a
np:Assertion
.
dgn-np:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_provenance
a
np:Provenance
.
dgn-np:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_assertion
{
miriam-gene:2253
a
ncit:C16612
.
lld:C0750929
a
ncit:C7057
.
dgn-gda:DGN55ddfb6af95dda8eafcf2271c87f7aee
sio:SIO_000628
miriam-gene:2253
,
lld:C0750929
;
a
sio:SIO_001121
.
}
dgn-np:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_provenance
{
dgn-np:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_assertion
dcterms:description
"[The genes selected are involved in signalling gradients occurring during segmental patterning of the occipital somites (FGF8, Wnt, and retinoic acid pathways and from bone morphogenetic proteins or BMP, Notch, Cdx and Hox pathways) or in placental angiogenesis, sclerotome development or CMI-associated syndromes.]. 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:23437350
;
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:NP413830.RAg2_bzfV8gKPOn9w9CtdPQMWiIi85HE1WdcijpBqszdU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:06+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" .
}