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- source_evidence_literature type ECO_0000212 NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion evidence source_evidence_literature NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion SIO_000772 19651702 NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion wasDerivedFrom befree-20150227 NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion wasGeneratedBy ECO_0000203 NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.