Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_provenance.
- NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_assertion description "[Mutations in the gene microcephalin/MCPH1 result in the neurodevelopmental disease microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_provenance.
- NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_assertion evidence source_evidence_literature NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_provenance.
- NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_assertion SIO_000772 22240477 NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_provenance.
- NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_assertion wasDerivedFrom befree-2016 NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_provenance.
- NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_assertion wasGeneratedBy ECO_0000203 NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_provenance.
- befree-2016 importedOn "2016-02-19" NP952838.RAIIa4tTA9L9jESN6civ3K1Qh10ItB4vIX2s6rODR_gpI130_provenance.