Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_assertion> ?p ?o ?g. }
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- NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_assertion type Assertion NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_head.
- NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_assertion description "[In addition, evidence for association to Asperger syndrome was observed with an intragenic single nucleotide polymorphism (SNP) of DISC1 (rs1322784; P=0.0058), as well as with a three-SNP haplotype (P=0.0013) overlapping the HEP3 haplotype, that was previously observed to associate with schizophrenia in Finnish families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_provenance.
- NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_assertion evidence source_evidence_literature NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_provenance.
- NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_assertion SIO_000772 17579608 NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_provenance.
- NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_assertion wasDerivedFrom befree-2016 NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_provenance.
- NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_assertion wasGeneratedBy ECO_0000203 NP616029.RA7-V13sS04ftV7vMdptpyEURPVLOTv9oMZ50GUApDQPI130_provenance.