@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q
> .
@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:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_head
{
this:
np:hasAssertion
dgn-np:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_assertion
;
np:hasProvenance
dgn-np:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_assertion
a
np:Assertion
.
dgn-np:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_provenance
a
np:Provenance
.
dgn-np:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_assertion
{
miriam-gene:5547
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGNaa68acf971233eaf6e5d95555eaebc94
sio:SIO_000628
miriam-gene:5547
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_provenance
{
dgn-np:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_assertion
dcterms:description
"[The chuzhoi mutant provides an additional genetic resource to help investigate the developmental basis of several congenital abnormalities including neural tube, heart and lung defects and their relationship to disruption of PCP.]. 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:20704721
;
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:NP876516.RAL10uCT8PPnUgbdBHuNnCib09FDAyPp6zR2Gb2f2of5Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:55+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" .
}