Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_provenance.
- NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_assertion description "[Here, we identified two de novo mutations in patients with sporadic SCZ in GRIN2A and one de novo mutation in GRIN2B in a patient with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_provenance.
- NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_assertion evidence source_evidence_literature NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_provenance.
- NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_assertion SIO_000772 22833210 NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_provenance.
- NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_assertion wasDerivedFrom befree-2016 NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_provenance.
- NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_assertion wasGeneratedBy ECO_0000203 NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1000430.RAobLjIEx0EHuVV3PIqFagyWMhKTiPTwZMHnm04zQxYIY130_provenance.