Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion> ?p ?o ?g. }
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- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion type Assertion NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_head.
- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_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." NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion evidence source_evidence_literature NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion SIO_000772 2683782 NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion wasDerivedFrom befree-20140225 NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion wasGeneratedBy ECO_0000203 NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.