Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_provenance.
- NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_assertion description "[We hypothesized that MCP mutations could predispose to HUS, and we sequenced MCP coding exons in affected individuals from 30 families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_provenance.
- NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_assertion evidence source_evidence_literature NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_provenance.
- NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_assertion SIO_000772 14566051 NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_provenance.
- NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_assertion wasDerivedFrom befree-20140225 NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_provenance.
- NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_assertion wasGeneratedBy ECO_0000203 NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP495057.RA-nqeK8XufyQ6HAnEm66UCFt3Gm4QLmotX1UqBmGI9PM130_provenance.