Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_provenance.
- NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_assertion description "[Novel INF2 mutation p. L77P in a family with glomerulopathy and Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_provenance.
- NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_assertion evidence source_evidence_literature NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_provenance.
- NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_assertion SIO_000772 22961558 NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_provenance.
- NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_assertion wasDerivedFrom befree-2016 NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_provenance.
- NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_assertion wasGeneratedBy ECO_0000203 NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1011471.RA1_oGt3KYmBHqVO_q-pZa8DQMSvQ8Asjuy_PkX1c0P-w130_provenance.