Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_provenance.
- NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_assertion wasGeneratedBy ECO_0000203 NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_provenance.
- NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_assertion wasDerivedFrom befree-20140225 NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_provenance.
- NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_assertion SIO_000772 11935336 NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_provenance.
- NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_assertion evidence source_evidence_literature NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_provenance.
- NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_assertion description "[We describe the analysis of the chromosome breakpoints in a patient with congenital bilateral isolated ptosis and a de novo balanced translocation 46,XY,t(1;8)(p34.3;q21.12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP404724.RA1tazNW8HIL7h3_FmLPEQbxC-nQHJFcNa6ktK7zkxJVk130_provenance.