Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion description "[Recent advances in genetics have resulted in the identification of missense mutations in TRPV4 in patients with these hereditary neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion evidence source_evidence_literature NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion SIO_000772 22187434 NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion wasDerivedFrom befree-2016 NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_assertion wasGeneratedBy ECO_0000203 NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.
- befree-2016 importedOn "2016-02-19" NP948331.RAPwX7w60o9_RUxtulj5pHnuTPHSqPIdDAVC_EKz2aSFo130_provenance.