Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_provenance.
- NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_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." NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_provenance.
- NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_assertion evidence source_evidence_literature NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_provenance.
- NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_assertion SIO_000772 7541290 NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_provenance.
- NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_assertion wasDerivedFrom befree-20140225 NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_provenance.
- NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_assertion wasGeneratedBy ECO_0000203 NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP848731.RAavCdg1c-KA-ugb2z8jjv-I2WHuu6ZQGabBCYJWbjYp4130_provenance.