Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_provenance.
- NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_assertion description "[In addition, a CDH7 mutation was found in an individual without temporal bone malformation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_provenance.
- NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_assertion evidence source_evidence_literature NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_provenance.
- NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_assertion SIO_000772 18445044 NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_provenance.
- NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_assertion wasDerivedFrom befree-20150227 NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_provenance.
- NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_assertion wasGeneratedBy ECO_0000203 NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP891312.RA1LALA9iFTgKNP25eh9WZyrd3NzBGTMI4WYlPagG-cKw130_provenance.