Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_assertion type Assertion NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_head.
- NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_assertion wasGeneratedBy ECO_0000203 NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_provenance.
- NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_assertion wasDerivedFrom befree-20150227 NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_provenance.
- NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_assertion SIO_000772 23428682 NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_provenance.
- NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_assertion evidence source_evidence_literature NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_provenance.
- NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_assertion description "[Patients with heterozygous mutations or deletions of IGF1R have a moderate pre- and postnatal growth failure, microcephaly and a history of feeding problems.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483102.RA8B_InXXYnUBJq4Spo4qfTArpL13mKQlxn8NEnGcgYq4130_provenance.