Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_provenance.
- NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_assertion description "[The X-linked type of HMSN is associated with defects of the connexin 32 gene, which encodes a gap junction protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_provenance.
- NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_assertion evidence source_evidence_literature NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_provenance.
- NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_assertion SIO_000772 7541290 NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_provenance.
- NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_assertion wasDerivedFrom befree-20150227 NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_provenance.
- NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_assertion wasGeneratedBy ECO_0000203 NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426084.RARDuDHYmuc2V50hUHBwTkNoMkF0dFm-KrBCKoB00wuY4130_provenance.