Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion description "[TSP-5 is of interest because mutations in the gene cause two skeletal dysplasias, pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED/EDM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion evidence source_evidence_literature NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion SIO_000772 18193163 NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion wasDerivedFrom befree-2016 NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_assertion wasGeneratedBy ECO_0000203 NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.
- befree-2016 importedOn "2016-02-19" NP649781.RA_3i38sFkEkSk6XkzVntgdBTgsmgfTxLjHJSj4_r6mLc130_provenance.