Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_provenance.
- NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_assertion description "[The second phenotype, observed in four unrelated families, is autosomal dominant trismus-pseudocamptodactyly syndrome (distal arthrogryposis type 7; previously associated exclusively with myosin heavy chain 8 mutations).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_provenance.
- NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_assertion evidence source_evidence_literature NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_provenance.
- NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_assertion SIO_000772 23413262 NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_provenance.
- NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_assertion wasDerivedFrom befree-20140225 NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_provenance.
- NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_assertion wasGeneratedBy ECO_0000203 NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP664730.RAbE7_R3qnnZDYYn7B15TRzJSult3vbdWbKz66aTaaN-I130_provenance.