Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_provenance.
- NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_assertion wasGeneratedBy ECO_0000203 NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_provenance.
- NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_assertion wasDerivedFrom befree-20150227 NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_provenance.
- NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_assertion SIO_000772 20507343 NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_provenance.
- NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_assertion evidence source_evidence_literature NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_provenance.
- NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_assertion description "[C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947828.RAMaSbDTF5rOpWJuUuzXrMCu9tHxJibR72e73wHcmVmAA130_provenance.