Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_assertion type Assertion NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_head.
- NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_assertion description "[A third PGRN sequence variation (R433W) was found in an FTD patient with family history of ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_provenance.
- NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_assertion evidence source_evidence_literature NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_provenance.
- NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_assertion SIO_000772 17202431 NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_provenance.
- NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_assertion wasDerivedFrom befree-2016 NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_provenance.
- NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_assertion wasGeneratedBy ECO_0000203 NP587115.RA-mCA9oOMdBL0qEj3xNQTElbwRZB9oWljI99HgF_wKlc130_provenance.