Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_provenance.
- NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_assertion wasGeneratedBy ECO_0000203 NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_provenance.
- NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_assertion wasDerivedFrom befree-20150227 NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_provenance.
- NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_assertion SIO_000772 19647026 NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_provenance.
- NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_assertion evidence source_evidence_literature NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_provenance.
- NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_assertion description "[So, HTR2A is unlikely to be a genetic marker for ASD in Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471363.RAvJT67Og-_VgLRsgt_5DvIUP-KBGI6svai0NxUXDu3aw130_provenance.