@prefix dc: . @prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_head { this: np:hasAssertion dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_assertion; np:hasProvenance dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_provenance; np:hasPublicationInfo dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_publicationInfo; a np:Nanopublication . dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_assertion a np:Assertion . dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_provenance a np:Provenance . dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_publicationInfo a np:PublicationInfo . } dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_assertion { miriam-gene:796 a ncit:C16612 . lld:C0004352 a ncit:C7057 . dgn-gda:DGNe93e7555795e5d6694670ee9115ff082 sio:SIO_000628 miriam-gene:796, lld:C0004352; a sio:SIO_001121 . } dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_provenance { dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_assertion dc:description "[In archived neonatal blood of children with autistic spectrum disorders (n = 69), mental retardation without autism (n = 60), or cerebral palsy (CP, n = 63) and of control children (n = 54), we used recycling immunoaffinity chromatography to measure the neuropeptides substance P (SP), vasoactive intestinal peptide (VIP), pituitary adenylate cyclase-activating polypeptide (PACAP), calcitonin gene-related peptide (CGRP), and the neurotrophins nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophin 3 (NT3), and neurotrophin 4/5 (NT4/5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_curated; sio:SIO_000772 miriam-pubmed:11357950; prov:wasDerivedFrom dgn-void:ctd_human-20130708; prov:wasGeneratedBy eco:ECO_0000218 . dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date . dgn-void:source_evidence_curated a eco:ECO_0000205; rdfs:comment "Gene-disease associations manually curated."@en; rdfs:label "DisGeNET evidence - CURATED"@en . } dgn-np:NP10448.RAjiiYGdHKHz_5waeMD0MQnuGn9pC0SwKoAincpEr3l9c130_publicationInfo { this: dc:created "2014-10-02T12:32:02+02:00"^^xsd:dateTime; dc:rights ; dc:rightsHolder dgn-void:IBIGroup; dc:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }