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- source_evidence_literature type ECO_0000212 NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_provenance.
- NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_assertion description "[In the field of the peripheral neuropathies we present data on a newly described autosomal recessive Charcot-Marie-Tooth disease (CMT4F) with mutations in the periaxin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_provenance.
- NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_assertion evidence source_evidence_literature NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_provenance.
- NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_assertion SIO_000772 12094560 NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_provenance.
- NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_assertion wasDerivedFrom befree-2016 NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_provenance.
- NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_assertion wasGeneratedBy ECO_0000203 NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_provenance.
- befree-2016 importedOn "2016-02-19" NP359380.RA2zqkwo6XyPQMYPl86e9Po6_3hyAJW7GsqNwePv1BGRI130_provenance.