Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_provenance.
- NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_assertion wasGeneratedBy ECO_0000203 NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_provenance.
- NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_assertion wasDerivedFrom befree-20150227 NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_provenance.
- NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_assertion SIO_000772 24179174 NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_provenance.
- NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_assertion evidence source_evidence_literature NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_provenance.
- NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_assertion description "[Inputs from genetic studies were provided through the identification of several mutated genes encoding either proteins associated with microtubules (DCX, LIS1, KIF2A, KIF5C, DYNC1H1) or tubulin subunits (TUBA1A, TUBB2B, TUBB5 and TUBG1), in malformations of cortical development (MCD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986896.RAVSWt7IsrJ9-zVSRidD67_gIfDBjYBOKObRSkFO_zAQI130_provenance.