Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_provenance.
- NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_assertion description "[BDNF and COMT may be biomarkers for phenotypic variation in ASD, but these preliminary findings remain tentative pending replication with larger, independent samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_provenance.
- NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_assertion evidence source_evidence_literature NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_provenance.
- NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_assertion SIO_000772 19582565 NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_provenance.
- NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_assertion wasDerivedFrom befree-2016 NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_provenance.
- NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_assertion wasGeneratedBy ECO_0000203 NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_provenance.
- befree-2016 importedOn "2016-02-19" NP749631.RATLXtexMTWFoj-Jekzvy187rpiRwLZFR3OByaMEvq4U0130_provenance.