@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs
> .
@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:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_head
{
this:
np:hasAssertion
dgn-np:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_assertion
;
np:hasProvenance
dgn-np:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_provenance
;
np:hasPublicationInfo
dgn-np:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_assertion
a
np:Assertion
.
dgn-np:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_provenance
a
np:Provenance
.
dgn-np:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_assertion
{
miriam-gene:4803
a
ncit:C16612
.
lld:C0003028
a
ncit:C7057
.
dgn-gda:DGNe4b680c12b8ab333a7600f3cfb4e2f34
sio:SIO_000628
miriam-gene:4803
,
lld:C0003028
;
a
sio:SIO_001121
.
}
dgn-np:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_provenance
{
dgn-np:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_assertion
dcterms:description
"[Human TRKA (NTRK1) encodes the receptor tyrosine kinases (RTKs) for nerve growth factor (NGF) and is the gene responsible for congenital insensitivity to pain with anhidrosis (CIPA), an autosomal recessive disorder characterized by a lack of pain sensation and anhidrosis.]. 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:11159935
;
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:NP318088.RAFnSwll1kz5HKFt5R6uRN9wRasWM-LSEDt3dYLoyzMqs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:04+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" .
}