Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_assertion> ?p ?o ?g. }
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- NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_assertion type Assertion NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_head.
- NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_assertion wasGeneratedBy ECO_0000203 NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_provenance.
- NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_assertion wasDerivedFrom befree-20140225 NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_provenance.
- NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_assertion SIO_000772 22509377 NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_provenance.
- NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_assertion evidence source_evidence_literature NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_provenance.
- NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_assertion description "[Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763104.RAFCwrOewxBdbp1dO82JNSKPcrIXpQ2hPvwULsAKcpX88130_provenance.