Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_provenance.
- NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_assertion description "[Mutation screening and DNA sequencing of the MET gene, which is mapped to 7q31, revealed only the presence of simple sequence polymorphisms but no apparent acquired disease-associated mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_provenance.
- NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_assertion evidence source_evidence_literature NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_provenance.
- NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_assertion SIO_000772 9485032 NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_provenance.
- NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_assertion wasDerivedFrom befree-20140225 NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_provenance.
- NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_assertion wasGeneratedBy ECO_0000203 NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP897409.RA6gmF3vVG6nOp6X5gd4XK2iWFgTkowQMYqrcyWbpGe9M130_provenance.