Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_provenance.
- NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_assertion description "[Here we present two additional patients with severe MR, autism spectrum disorder and epilepsy, carrying a very small deletion encompassing the MEF2C gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_provenance.
- NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_assertion evidence source_evidence_literature NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_provenance.
- NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_assertion SIO_000772 20412115 NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_provenance.
- NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_assertion wasDerivedFrom befree-20140225 NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_provenance.
- NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_assertion wasGeneratedBy ECO_0000203 NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP895226.RA_9qU3qnqxrhBhikP3-xlTFDLob8mUuA2JTMIHOaUYiE130_provenance.