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- source_evidence_literature type ECO_0000212 NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_provenance.
- NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_assertion description "[The presence of mutations in the ALK-1 gene in ten patients with underlying connective tissue diseases was investigated ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_provenance.
- NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_assertion evidence source_evidence_literature NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_provenance.
- NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_assertion SIO_000772 16941203 NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_provenance.
- NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_assertion wasDerivedFrom lhgdn-20090331 NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_provenance.
- NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_assertion wasGeneratedBy ECO_0000203 NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP219303.RAgHF9-D9bvzcfLyFlnNTXg0LpxGpzz6G-elOybsNnrG8130_provenance.