Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_provenance.
- NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_assertion description "[Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_provenance.
- NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_assertion evidence source_evidence_literature NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_provenance.
- NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_assertion SIO_000772 10878661 NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_provenance.
- NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_assertion wasDerivedFrom befree-2016 NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_provenance.
- NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_assertion wasGeneratedBy ECO_0000203 NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_provenance.
- befree-2016 importedOn "2016-02-19" NP287986.RANahPc2JUKN6HRVrOBdCDPc4Lbl6LMbQaia_Is7XS2as130_provenance.