Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_provenance.
- NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_assertion description "[The conclusion that most variants of OI are caused by mutations in the structural genes for type I procollagen has broad implications for other diseases that affect connective tissue, diseases such as chondrodystrophies, osteoarthritis, and osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_provenance.
- NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_assertion evidence source_evidence_literature NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_provenance.
- NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_assertion SIO_000772 2683782 NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_provenance.
- NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_assertion wasDerivedFrom befree-20140225 NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_provenance.
- NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_assertion wasGeneratedBy ECO_0000203 NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP917833.RAWf3H7ejmnMoWC814_MyXx1qRwABZK33uklalKW_pZ-c130_provenance.