Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_provenance.
- NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_assertion description "[RAB7 mutations were only found in patients with a Charcot-Marie-Tooth type 2B (CMT2B) phenotype, an axonal sensory-motor neuropathy with pronounced ulcero-mutilations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_provenance.
- NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_assertion evidence source_evidence_literature NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_provenance.
- NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_assertion SIO_000772 19651702 NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_provenance.
- NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_assertion wasDerivedFrom befree-20140225 NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_provenance.
- NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_assertion wasGeneratedBy ECO_0000203 NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP642775.RAxHTr1-zbQM7k98bjChPV21gTPxZD7nW5V0W2ZPBB5bI130_provenance.