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- source_evidence_literature type ECO_0000212 NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_provenance.
- NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_assertion description "[The MPZ role in the pathogenesis of both demyelinating and axonal inherited neuropathies was evaluated in the Italian population by screening a cohort of 214 patients with CMT1 or CMT2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_provenance.
- NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_assertion evidence source_evidence_literature NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_provenance.
- NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_assertion SIO_000772 19293842 NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_provenance.
- NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_assertion wasDerivedFrom befree-2016 NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_provenance.
- NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_assertion wasGeneratedBy ECO_0000203 NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_provenance.
- befree-2016 importedOn "2016-02-19" NP726747.RAjwO1HxtRYXt4hvgFgnb8Zz6qxmi53n52QEkgt5zdDxw130_provenance.