@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8
> .
@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:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_head
{
this:
np:hasAssertion
dgn-np:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion
;
np:hasProvenance
dgn-np:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_provenance
;
np:hasPublicationInfo
dgn-np:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion
a
np:Assertion
.
dgn-np:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_provenance
a
np:Provenance
.
dgn-np:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion
{
miriam-gene:4488
a
ncit:C16612
.
lld:C1868598
a
ncit:C7057
.
dgn-gda:DGN8874049d0fe48591a7c223a801b6e380
sio:SIO_000628
miriam-gene:4488
,
lld:C1868598
;
a
sio:SIO_001121
.
}
dgn-np:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_provenance
{
dgn-np:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_assertion
dcterms:description
"[Mutation analysis of the ALX4 gene in three unrelated FPP families without the MSX2 mutation identified mutations in two families, indicating that mutations in ALX4 could be responsible for these skull defects and suggesting further genetic heterogeneity of FPP.]. 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:11106354
;
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:NP571845.RAOEFhwBdgmQHgrbCoFSK6JmoBqIqy2H5Sj-lTDZj0el8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:20+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" .
}