Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance.
- NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance.
- NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_assertion evidence source_evidence_literature NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance.
- NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_assertion SIO_000772 19651702 NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance.
- NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_assertion wasDerivedFrom befree-20150227 NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance.
- NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_assertion wasGeneratedBy ECO_0000203 NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance.