Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_provenance.
- NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_assertion description "[Inherited and de novo SHANK2 variants associated with autism spectrum disorder impair neuronal morphogenesis and physiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_provenance.
- NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_assertion evidence source_evidence_literature NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_provenance.
- NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_assertion SIO_000772 21994763 NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_provenance.
- NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_assertion wasDerivedFrom befree-20150227 NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_provenance.
- NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_assertion wasGeneratedBy ECO_0000203 NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP866242.RAT3d4j8qxTwAQJPMcqQXZDXNr-2l3ynEdC6JgJ9r0YGI130_provenance.