Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_provenance.
- NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_assertion description "[Lack of functional stereocilin and CATSPER2 (a voltage-gate cation channel expressed specifically in spermatozoa) may explain the observed deafness and male infertility phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_provenance.
- NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_assertion evidence source_evidence_literature NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_provenance.
- NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_assertion SIO_000772 12825070 NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_provenance.
- NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_assertion wasDerivedFrom befree-2016 NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_provenance.
- NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_assertion wasGeneratedBy ECO_0000203 NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_provenance.
- befree-2016 importedOn "2016-02-19" NP399475.RAibRvgWeAMZQWaHL6vW60bCPN4VH4XdLRI9VAnl4FwJE130_provenance.