Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_assertion> ?p ?o ?g. }
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- NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_assertion type Assertion NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_head.
- NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_assertion description "[The aim of this study was to determine how often hematuria in families with TBMD segregated with haplotypes at the chromosomal loci for autosomal recessive and X-linked Alport syndrome (COL4A3/COL4A4 and COL4A5, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_provenance.
- NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_assertion evidence source_evidence_literature NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_provenance.
- NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_assertion SIO_000772 11318937 NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_provenance.
- NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_assertion wasDerivedFrom befree-20150227 NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_provenance.
- NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_assertion wasGeneratedBy ECO_0000203 NP320031.RARFy0LvoKll1tjEJnlfCniIuESMpC8FhBUseueaXQ4RA130_provenance.