@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0
> .
@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/v4.0.0/void/
> .
dgn-np:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_head
{
this:
np:hasAssertion
dgn-np:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_assertion
;
np:hasProvenance
dgn-np:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_provenance
;
np:hasPublicationInfo
dgn-np:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_assertion
a
np:Assertion
.
dgn-np:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_provenance
a
np:Provenance
.
dgn-np:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_assertion
{
miriam-gene:3897
a
ncit:C16612
.
lld:C3536983
a
ncit:C7057
.
dgn-gda:DGNc4555552e710967a8512c0d53b31d6a1
sio:SIO_000628
miriam-gene:3897
,
lld:C3536983
;
a
sio:SIO_001121
.
}
dgn-np:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_provenance
{
dgn-np:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_assertion
dcterms:description
"[While it is obvious that additional studies are necessary to further delineate the association between XLH and HSCR in the presence of L1CAM mutations, the documentation of this new patient reinforces the role of this gene acting either in a direct or indirect way in the pathogenesis of Hirschsprung disease.]. 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:22344793
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP961755.RAo3eT4WicVwYHgcA7esnCwkDO6NUf5j5gQLFJdiQVri0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:01+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}