Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_assertion type Assertion NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_head.
- NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_assertion description "[Hereditary protein C deficiency associated with mutations in exon IX of the protein C gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_provenance.
- NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_assertion evidence source_evidence_literature NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_provenance.
- NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_assertion SIO_000772 7831652 NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_provenance.
- NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_assertion wasDerivedFrom gad-20130706 NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_provenance.
- NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_assertion wasGeneratedBy ECO_0000203 NP52670.RAFgTxzts5lF4IOQUkHMIsphP4wFJDsetgnv0schZxBNI130_provenance.